Alaris SE DFU V8.5 7131 User Manual

User Manual: Alaris 7131 User Manual

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Alaris® Products

Directions for Use

Alaris® SE Pump

Models 7130/7131 and 7230/7231

Supports Guardrails® Suite MX

June 2006

OPTION

SEC

PRI

POWER

RUN

HOLD

Clear Enter

PRI SEC HLD OPT KVO

HLD PRI SECKVO OPT

456

789

•0

POWER

RUN

HOLD

A B

ml/hr ml/hr

SEC

PRI

Clear Enter

OPT PRI HLD SEC KVO

RUN

HOLD

POWER

OPTIONS

456

789

ml/hr

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7320/7231

General Contact Information

For service contact your local Affiliate Office or Distributor.

Cardinal Health,

PO Box 5527,

Dubai, United Arab Emirates.

Tel: (971) 4 28 22 842

Fax: (971) 4 28 22 914

Cardinal Health,

Pascalstr. 2,

52499 Baesweiler,

Deutschland.

Tel: (49) 2401 604 0

Fax: (49) 2401 604 121

Cardinal Health,

Via Ticino 4,

50019 Sesto Fiorentino,

Firenze, Italia.

Tél: (39) 055 30 33 93 00

Fax: (39) 055 34 00 24

Cardinal Health

10221 Wateridge Circle,

San Diego, CA 92121,

USA.

Tel: (1) 800 854 7128

Fax: (1) 858 458 6179

Cardinal Health,

8/167 Prospect Highway,

Seven Hills, NSW 2147,

Australia.

Tel: (61) 2 9838 0255

Fax: (61) 2 9674 4444

Fax: (61) 2 9624 9030

Cardinal Health,

Avenida Valdeparra 27,

28108 - Alcobendas, Madrid,

España.

Tel: (34) 91 657 20 31

Fax: (34) 91 657 20 42

Cardinal Health,

Kantorenpand “Hoefse Wing”,

Printerweg, 11,

3821 AP Amersfoort,

Nederland.

Tel: (31) 33 455 51 00

Fax: (31) 33 455 51 01

Cardinal Health,

Unit 2 Oude Molen Business

Park,

Oude Molen Road, Ndabeni,

Cape Town 7405, South Africa.

Tel: (27) (0) 860 597 572

Tel: (27) 21 510 7562

Fax: (27) 21 5107567

Cardinal Health,

Otto De Mentockplein 19,

1853 Strombeek - Bever,

Belgium.

Tel: (32) 2 267 38 99

Fax: (32) 2 267 99 21

Cardinal Health,

Immeuble Antares - Technoparc,

2, rue Charles-Edouard Jeanneret.

78300 POISSY,

France.

Tél: (33) 1 30 06 74 60

Fax: (33) 1 39 11 48 34

Cardinal Health

Solbråveien 10 A,

1383 ASKER,

Norge.

Tel: (47) 66 98 76 00

Fax: (47) 66 98 76 01

Cardinal Health,

235 Shields Court,

Markham,

Ontario L3R 8V2,

Canada.

Tel: (1) 905-752-3333

Fax: (1) 905-752-3343

Cardinal Health,

The Crescent, Jays Close,

Basingstoke,

Hampshire, RG22 4BS,

United Kingdom.

Tel: (44) 0800 917 8776

Fax: (44) 1256 330860

Cardinal Health,

14 George Bourke Drive

Mt Wellington, Auckland

PO Box 14234

Panmure, Auckland

Tel: 09 270 2420

Freephone: 0508 422734

Fax: 09 270 6285

Cardinal Health,

Shanghai Representative Office,

Suite 9B,

Century Ba-Shi Building,

398 Huai Hai Rd(M.),

Shanghai 200020,

China.

Tel: (56) 8621-63844603

Tel: (56) 8621-63844493

Fax: (56) 8621-6384-4025

Cardinal Health,

Döbrentei tér 1,

H-1013 Budapest,

Magyarország.

Tel: (36) 14 88 0232

Tel: (36) 14 88 0233

Fax: (36) 12 01 5987

Cardinal Health,

Hammarbacken 4B,

191 46 Sollentuna,

Sverige.

Tel: (46) 8 544 43 200

Fax: (46) 8 544 43 225

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Table of Contents

GETTING STARTED

INTRODUCTION ................................................................................................................................................................................................ 1

UNPACKING ......................................................................................................................................................................................................... 3

CHECK-IN AND CONFIGURATION .......................................................................................................................................................... 4

Rate Accuracy Qualification Test ...................................................................................................................................................... 4

Alternative Rate Accuracy Qualification Test .............................................................................................................................. 8

Set Sensor Check / Pressure Calibration Verification ............................................................................................................. 11

Functional Test .......................................................................................................................................................................................... 11

Flow Stop Test ........................................................................................................................................................................................... 13

Ground Current Leakage Test ............................................................................................................................................................ 13

Ground Resistance Test ....................................................................................................................................................................... 13

Instrument Configuration ...................................................................................................................................................................... 13

ADMINISTRATION SET INFORMATION ................................................................................................................................................ 14

General ......................................................................................................................................................................................................... 14

SmartSite® Infusion Set ......................................................................................................................................................................... 14

Preparing Solution Container and Set ............................................................................................................................................ 15

Loading Set ................................................................................................................................................................................................ 16

Removing Set ............................................................................................................................................................................................ 18

Changing Solution Container .............................................................................................................................................................. 18

PROGRAMMING

PROGRAMMING AND NAVIGATION TIPS ........................................................................................................................................... 19

Soft Keys ..................................................................................................................................................................................................... 19

Entering Values ......................................................................................................................................................................................... 19

Menus - With Guardrails® Suite MX Protection .......................................................................................................................... 20

Menus - NO Guardrails® Suite MX Protection ............................................................................................................................. 21

Split Screen (Dual Channel Only) ..................................................................................................................................................... 21

Powering On and Off .............................................................................................................................................................................. 21

Responding to Maintenance Reminder .......................................................................................................................................... 23

Responding to Time Set Reminder .................................................................................................................................................. 23

GUARDRAILS® SUITE MX PROMPTS .................................................................................................................................................... 24

Soft Limits ................................................................................................................................................................................................... 24

Hard Limits .................................................................................................................................................................................................. 24

PRIMARY INFUSION - WITH GUARDRAILS® SUITE MX PROTECTION .............................................................................. 25

Selecting New Patient and Profile Options ................................................................................................................................... 25

Primary Infusion Introduction ............................................................................................................................................................. 27

Continuous Infusion ................................................................................................................................................................................ 27

Pausing and Restarting Infusion ....................................................................................................................................................... 31

Making Changes During Continuous Infusion ............................................................................................................................. 31

Resuming Interrupted Infusion ........................................................................................................................................................... 32

KVO Mode .................................................................................................................................................................................................. 33

Resuming Operation from KVO Mode ............................................................................................................................................ 34

Clearing Volume Infused ...................................................................................................................................................................... 34

Bolus Dose ................................................................................................................................................................................................. 34

Delivering a Bolus Dose Prior to Beginning Continuous Infusion ...................................................................................... 35

Delivering a Bolus Dose During a Continuous Infusion .......................................................................................................... 36

Bolus Only ................................................................................................................................................................................................... 37

Stopping Bolus Dose .............................................................................................................................................................................. 39

Repeating a Bolus Dose ....................................................................................................................................................................... 39

Intermittent Infusion ................................................................................................................................................................................ 40

Making Changes During Intermittent Infusion ............................................................................................................................. 43

IV Fluid Infusion ........................................................................................................................................................................................ 44

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

ii Table of Contents

PROGRAMMING (Continued)

SECONDARY INFUSION - WITH GUARDRAILS® SUITE MX PROTECTION ...................................................................... 46

Introduction ................................................................................................................................................................................................. 46

Setup ............................................................................................................................................................................................................. 47

Secondary Intermittent Infusion ........................................................................................................................................................ 48

PRIMARY INFUSION - NO GUARDRAILS® SUITE MX PROTECTION ................................................................................... 52

Selecting New Patient Option-Profiles Feature Not Enabled (OFF) ................................................................................. 52

Basic Infusion ............................................................................................................................................................................................ 52

Promoting Basic Infusion to Guardrails® Suite MX Protection Infusion ........................................................................... 53

Promoting Basic Infusion to Guardrails® Drug Infusion .......................................................................................................... 53

Promoting Basic Infusion to Guardrails® IV Fluid Infusion ..................................................................................................... 55

Dose Rate Calculation- Drug? NO DOSE LIMIT-Profiles Feature Enabled (ON) ....................................................... 56

Dose Rate Calculation- Drug? NO DOSE LIMIT-Profiles Feature Not Enabled (OFF) ............................................ 58

LOADING DOSE ................................................................................................................................................................................................. 61

Programming ............................................................................................................................................................................................. 61

MULTI-DOSE ........................................................................................................................................................................................................ 63

Resuming an Interrupted Multi-Dose .............................................................................................................................................. 68

MULTI-STEP ......................................................................................................................................................................................................... 69

Making Changes During Multi-Step ................................................................................................................................................. 75

Resuming an Interrupted Multi-Step ............................................................................................................................................... 78

QUITTING MULTI-DOSE AND MULTI-STEP ....................................................................................................................................... 79

SECONDARY INFUSION - NO GUARDRAILS® SUITE MX PROTECTION ........................................................................... 80

Basic Secondary Infusion-Profiles Feature Enabled (On) ..................................................................................................... 80

Basic Secondary Infusion-Profiles Feature Not Enabled (Off) ............................................................................................ 81

DYNAMIC MONITORING SYSTEM

MONITORING OPTIONS - GENERAL ..................................................................................................................................................... 83

Selecting Monitoring Option ................................................................................................................................................................ 84

MONITORING OPTIONS - RESISTANCE MODE .............................................................................................................................. 86

Detection of Downstream Occlusions ............................................................................................................................................. 86

Auto Restart Plus Feature .................................................................................................................................................................... 87

Resistance Alert ....................................................................................................................................................................................... 88

Resistance Trend Graphs .................................................................................................................................................................... 89

MONITORING OPTIONS - PRESSURE MODE .................................................................................................................................. 92

Detection of Downstream Occlusions ............................................................................................................................................. 92

Auto Restart Plus Feature .................................................................................................................................................................... 92

Adjustable Pressure Alarm .................................................................................................................................................................. 93

Pressure Baseline ................................................................................................................................................................................... 95

Pressure Trend Graphs ......................................................................................................................................................................... 97

UPSTREAM OCCLUSION DETECTION ................................................................................................................................................. 100

GENERAL SETUP AND OPERATION

AUDIO ADJUST .................................................................................................................................................................................................. 103

TAMPER RESIST ............................................................................................................................................................................................... 103

Locking and Unlocking Panel Lock .................................................................................................................................................. 103

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

iii

Table of Contents

GENERAL INFORMATION

WARNINGS AND CAUTIONS ...................................................................................................................................................................... 105

Guardrails® Suite MX ............................................................................................................................................................................. 106

Administration Sets ................................................................................................................................................................................. 107

Epidural Administration ......................................................................................................................................................................... 107

Electromagnetic Compatibility ............................................................................................................................................................ 108

BATTERY MANAGEMENT SYSTEM ........................................................................................................................................................ 109

Battery Power Gauge and Indicator ................................................................................................................................................ 110

Battery Recharge ..................................................................................................................................................................................... 110

FLOW SENSOR .................................................................................................................................................................................................. 110

ALERTS COUNTER .......................................................................................................................................................................................... 112

Definitions ................................................................................................................................................................................................... 112

Viewing Alerts Counter ......................................................................................................................................................................... 113

NURSE CALL (7130/7230 ONLY) ............................................................................................................................................................... 114

Activating Nurse Call Feature ............................................................................................................................................................. 114

If an Alarm Occurs .................................................................................................................................................................................. 114

POLE CLAMP ...................................................................................................................................................................................................... 115

Changing Pole Clamp Orientation .................................................................................................................................................... 115

RS-232 COMPUTER LINK ............................................................................................................................................................................. 116

Connecting to a Computer ................................................................................................................................................................... 116

Disconnecting from a Computer ....................................................................................................................................................... 117

FEATURES AND DISPLAYS ......................................................................................................................................................................... 118

Operating Features, Controls, Indicators ...................................................................................................................................... 118

Displays ........................................................................................................................................................................................................ 121

Feature Definitions .................................................................................................................................................................................. 122

CONFIGURABLE SETTINGS ...................................................................................................................................................................... 123

Configurable Option Definitions-General ...................................................................................................................................... 124

Configurable Option Definitions-Guardrails® Suite MX ........................................................................................................... 128

Configurable Options ............................................................................................................................................................................. 129

System Configurable Options ............................................................................................................................................................ 130

SPECIFICATIONS .............................................................................................................................................................................................. 130

SYMBOLS AND TERMS ................................................................................................................................................................................. 134

TRUMPET AND START-UP CURVES ..................................................................................................................................................... 137

Pressure Mode .......................................................................................................................................................................................... 138

Resistance Mode ..................................................................................................................................................................................... 140

High Resistance Mode .......................................................................................................................................................................... 142

TROUBLESHOOTING AND MAINTENANCE

GENERAL .............................................................................................................................................................................................................. 143

AIR IN LINE ASSEMBLY ................................................................................................................................................................................. 143

SINGLE OR ACCUMULATED AIR BUBBLE DETECTION (NO RESET FEATURE) .......................................................... 144

ALARMS, ALERTS, PROMPTS .................................................................................................................................................................. 145

Alarms ........................................................................................................................................................................................................... 146

Alerts ............................................................................................................................................................................................................. 150

Prompts ........................................................................................................................................................................................................ 151

INSPECTION REQUIREMENTS ................................................................................................................................................................. 156

CLEANING ............................................................................................................................................................................................................ 156

SERVICE INFORMATION .............................................................................................................................................................................. 158

Technical Support .................................................................................................................................................................................... 158

WARRANTY ......................................................................................................................................................................................................... 159

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

iv Table of Contents

REGULATIONS AND STANDARDS

COMPLIANCE ..................................................................................................................................................................................................... 161

Electromagnetic Environment ............................................................................................................................................................ 161

Standards .................................................................................................................................................................................................... 168

TRADEMARKS .................................................................................................................................................................................................... 168

DIRECTIONS FOR USE SUPPLEMENTS

SUPPLEMENTS................................................................................................................................................ 169

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

Introduction

This document provides directions for use for the SE Pump,

Models 7130/7131 and 7230/7231. It is used in conjunction

with:

Alaris® product administration set instructions

Drug product labeling

SE Pump Technical Service Manual

Ground test equipment instructions

ECG monitoring system instructions

The SE Pump is intended for use in professional healthcare

environments, including healthcare facilities, home care, and

medical transport, that utilize infusion pumps for the delivery of

fluids, medications, blood, and blood products. It is indicated

for continuous or intermittent delivery through clinically

acceptable routes of administration; such as, intravenous

(IV), intra-arterial (IA), subcutaneous, epidural, enteral, and

irrigation of fluid spaces.

The SE Pump is available as either a single or a dual channel

pump that supports the Guardrails® Suite MX. The SE Dual

Channel Pump is a two-channel device intended to deliver

multiple infusions to a single patient.

Guardrails® Suite MX for the SE Pump brings a new level

of medication error prevention to the point of patient care.

Guardrails® Suite MX features programming guidelines for

medication dosing, delivery rate, duration, bolus dose and

bolus dose administration rate, concentration and optional

initial programming values in up to 15 patient-specific care

areas referred to as profiles. Each profile contains a specific

Drug Library and an IV Fluid library as well as instrument

configurations appropriate for the care area. Optional drug-

specific or fluid-specific clinical advisories provide visual

messages. Limits for each Guardrails® drug or fluid entry may

include Hard Limits that cannot be overridden during infusion

programming and/or Soft Limits that can be overridden, based

on clinical requirements.

A Data Set is developed and approved by the facility’s own

multi-disciplinary team using the Editor Software, the PC-

based authoring tool. A Data Set is then transferred to the

SE Pump by qualified personnel. Approved Data Sets are

maintained by the Editor Software for future updates and

reference.

CAUTION

WARNING

Read all instructions before using

the SE Pump.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

2Getting Started

Information about a Guardrails® alert that occurs during use

is stored within the SE Pump, and can be accessed using the

CQI Reporter.

The SE Pump may be operated with or without the Guardrails®

Suite MX protection. When an approved Data Set is

transferred to the SE Pump by qualified personnel and the

Profiles feature is enabled (ON) in instrument configuration,

then Guardrails® Suite MX protection is available. When

the Profiles feature is not enabled (Off), or when no Data

Set has been transferred to the SE Pump, Guardrails® Suite

MX protection is not available (see "Primary Infusion – NO

Guardrails® Suite MX Protection", and "Secondary Infusion

- NO Guardrails® Suite MX Protection"). Programming and

navigation may differ when Guardrails® Suite MX software is

not in use.

Documentation provided with this product may reference

product not present in your facility or not yet available for sale

in your area.

A superscript number (for example, À) identifies additional

information provided as a note at the end of the section.

Administration Sets: Reference “General Information” for

specific “Administration Set Information”.

Alarms, Alerts, Prompts: Reference “Troubleshooting and

Maintenance” for specific alarms, alerts and prompts.

Electromagnetic Environment: Reference “Regulations and

Standards”, "Compliance”.

Contraindications: None known.

Warnings and Cautions:

Warnings and cautions provide information needed to safely and

effectively use the SE Pump. Reference "General Information",

"Warnings and Cautions".

A DANGER is an alert to an imminent hazard which

could result in serious personal injury and/or product damage

if proper procedures are not followed.

A WARNING is an alert to a potential hazard which could

result in serious personal injury and/or product damage if

proper procedures are not followed.

Introduction (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

1. Remove instrument from carton.

2. Important: Plug instrument into an AC outlet a minimum

of 24 hours prior to use.

Maximum battery capacity, as well as gauge accuracy, is

reached after several charge/discharge/recharge cycles,

in the refresh process. Cardinal Health recommends that

the battery be fully charged/discharged/recharged, using

the refresh cycle, before placing the instrument in use.

3. Perform Periodic Inspections (reference "Troubleshooting

and Maintenance", “Inspection Requirements”).

See "General Information", "Configurable Settings" for a list of

the configurable features.

WARNING

Failure to properly charge the

battery results in an instrument

malfunction. Biomedical personnel

in the facility are responsible for

unpacking the instrument and

ensuring the battery is fully charged

before placing the instrument in use.

Unpacking

Introduction (Continued)

Warnings and Cautions: (Continued)

A CAUTION is an alert to a potential hazard which could

result in minor personal injury and/or product damage if proper

procedures are not followed.

DEFINED TERMS:

The following table identifies the defined terms used

throughout this document for certain products and product

features.

Product Name Defined Term

AccuSlide® flow regulator Flow Regulator

Alaris® SE pump SE Pump

Guardrails® clinical advisory Clinical Advisory

Guardrails® CQI Reporter CQI Reporter

Guardrails® data set Data Set

Guardrails® drug library Drug Library

Guardrails® Editor Editor Software

Guardrails® hard limit Hard Limit

Guardrails® IV fluid IV Fluid

Guardrails® soft limit Soft Limit

SmartSite® needle-free valve Needle-Free Valve

SmartSite® positive bolus needle-free valve Needle-Free Valve

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

4Getting Started

Rate Accuracy Qualification Test

This procedure is to be used only for the testing of an

instrument during New Instrument Check-In or when just

received from the Service Depot Center. This test is to verify

that damage or changes to the instrument did not occur during

shipment and handling.

Rate accuracy should be tested using a Model 80VCS

Calibration Set. The system is designed to produce overall

accuracy of ±5% for rates greater than 1 mL/h and up to

999.9 mL/h, and ±6.5% for rates equal to or less than 1 mL/h,

95% of the time with 95% confidence (reference "General

Information", "Trumpet and Start-Up Curves" for additional

information). The system performance with a calibration

set produces a smaller variability. In order to ensure overall

accuracy is achieved, new instruments are tested to an

accuracy of ±3% with the Model 80VCS set during New

Instrument Check-In.

Due to the dynamic monitoring feature, the rate is varied during

operation. For this reason, automatic testers should not be

used to check rate accuracy. Generally, these devices collect

small samples and may cause the results to be incorrect, even

though the instrument is accurate.

This is a quick reference procedure for check-in and

configuration of new and recently serviced instruments.

Check-In and Configuration

WARNING

Instruments returned from the

service depot may be set to

factory defaults and not have a

hospital-defined Data Set loaded.

Biomedical personnel in the facility

are responsible for checking-in the

instrument and ensuring the current

hospital-approved Data Set is

loaded.

CAUTION

Charge the battery for a minimum

of 24 hours prior to performing

the check-in and configuration

procedures. Batteries without

a full charge on initial use may

become damaged and/or cause a

malfunction.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

Rate Accuracy Qualification Test (Continued)

able or Bench

30 ±1 in

76.2 cm±2.5

Water Source

80VCS Calibration Set

Instrument Stand

Used Fluid Receptacle

IV Tubing Three-Way

Stopcock

Burette (50 ml)

Burette Clamp

Equipment Stand

Table or Bench

Test Setup

1. Fill solution container with clean tap water. Close Flow

Regulator clamp on 80VCS set and then insert spike into

solution container.

2. Open Flow Regulator clamp and prime set. Ensure all air

is expelled from set. Close Flow Regulator clamp.

3. Connect output of set to one side of three-way stopcock.

4. Load set into instrument.

Check-In and Configuration (Continued)

Do not use the Model 80VCS Calibration Set for more than

30 rate verification runs (15 rate calibration number changes).

Keep track of the number of times the set is used by recording

each use on the 80VCS insert or on a separate record.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

6Getting Started

Check-In and Configuration (Continued)

Rate Accuracy Qualification Test (Continued)

5. Close latch.

6. Verify no fluid flow or drops falling in drip chamber.

7. Plug instrument into a properly grounded AC outlet.

8. Set stopcock to output into a class A or B burette.

9. Press POWER key to turn channel on.

10. Set primary infusion rate to 400 mL/h.

11. Set VTBI to 20 mL.

12. Ensure instrument (both channels if dual channel) is set to

Pressure mode. À

13. Press RUN/HOLD key to start primary infusion. Infuse

until tubing and burette are fully primed (approximately 1

minute).

14. Press RUN/HOLD key to stop infusion.

15. Adjust height of instrument and/or fluid container to attain

a head height of 30 ±1 inches / 76.2 ±2.5 centimeters

between middle of pumping mechanism and fluid level in: Á

• bag or vented bottle (vent closed on administration set)

• drip chamber (unvented bottle with vent open on

administration set).

16. Adjust fluid level in burette until meniscus is level with zero

mark on burette. Â

17. Verify primary infusion rate is 400 mL/h.

18. Reset VTBI to 40 mL and clear volume infused.

19. Press RUN/HOLD key to start primary infusion.

20. Instrument will run approximately 360 seconds (6 minutes)

to complete delivery and then go into KVO mode. Stop

instrument within 1 second of its entering KVO mode.

21. Make a note of volume collected in burette.

22. Note expected volume, as identified on 80VCS set insert.

23. Do not remove 80VCS set from instrument until one of

following conclusions is determined:

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

Rate Accuracy Qualification Test (Continued)

• Instrument passes rate verification and calibration is

not needed.

• Rate calibration number was changed and instrument

now passes verification.

• Mechanism replacement is required.

24. Calculate volume accuracy, as follows:

Volumetric Volume Accuracy Error Computation

Vcollected = volume in burette in milliliters

Vexpected = characterized volume printed on 80VCS set

insert

Step 1: A = Vcollected ÷ Vexpected

Step 2: B = A x 100

Step 3: % Error (round % Error to nearest tenth of a percent)

= B – 100

25. Result should be 0.0±3%.

26. If volume accuracy does not fall within required range of

±3% from expected volume and test results were:

• inside a range of -5.5% to +7.0% from expected

volume,

perform rate calibration (reference Technical Service

Manual). Set rate calibration number to 0.0% before

running rate test, to determine a new calibration

number.

• outside a range of -5.5% to +7.0% from expected

volume,

return instrument to Cardinal Health for repair or

replace mechanism.

27. Set stopcock to drain fluid in burette to zero level, in

preparation for next test.

NOTES:

À The factory default for the Monitoring Options mode is

Pressure.

Á A 30-inch head height was used in the initial qualification of

this process and is the recommended head height for the

Check-In Rate Accuracy Test. Based on observed field use, a

24-inch head height was also tested and verified for the Rate

Accuracy Specification.

Â The instrument may need to be run to prime the line to the

zero level of the burette (step 13).

Check-In and Configuration (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

8Getting Started

Alternative Rate Accuracy Qualification Test

Check-In and Configuration (Continued)

This procedure is to be used only for the testing of an

instrument during New Instrument Check-In or when just

received from the Service Depot Center. This test is to verify

that damage or changes to the instrument did not occur during

shipment and handling.

Make the following changes to Test Setup:

• Burette and equipment stand have been replaced by digital

scale, Acculab Vic-212 or equivalent and 50 or 100 mL

flask (plastic or glass).

• Three-way stopcock and used fluid receptacle are no

longer needed.

Due to the dynamic monitoring feature, the rate is varied

during operation. For this reason, Cardinal Health does not

recommend using automatic testers to check rate accuracy.

Generally, these devices collect small samples and may cause

the results to be incorrect, even though the instrument is

accurate.

Do not use the Model 80VCS set for more than 30 rate

verification runs (15 rate calibration number changes). Keep

track of the number of times the set is used by recording each

use on the 80VCS insert or on a separate record.

1. Fill solution container with clean tap water. Close Flow

Regulator clamp on 80VCS Calibration Set and then insert

spike into solution container.

2. Open Flow Regulator clamp and prime set. Ensure all air

is expelled from set. Close Flow Regulator clamp.

3. Place flask in middle of scale.

4. Load set into instrument.

5. Close latch.

6. Verify no fluid flow or drops falling in drip chamber.

7. Plug instrument into a properly grounded AC outlet.

8. Place output of set so it drips into flask. (Do not let set rest

on flask.)

9. Press channel’s POWER switch to turn channel on.

10. Set primary infusion rate to 400 mL/h.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

Alternative Rate Accuracy Qualification Test (Continued)

Check-In and Configuration (Continued)

11. Set VTBI to 20 mL.

12. Ensure instrument (both channels if dual channel) is set to

Pressure mode. À

13. Press RUN/HOLD key to start primary infusion. Infuse

until tubing is fully primed (approximately 1 minute).

14. Press RUN/HOLD key to stop infusion.

15. Adjust height of instrument and/or fluid container to attain

a head height of 30 ±1 inches between middle of pumping

mechanism and fluid level in:

• bag or vented bottle (vent closed on administration set)

• drip chamber (unvented bottle with vent open on

administration set).

16. Zero reading on scale.

17. Verify primary infusion rate is 400 mL/h.

18. Reset VTBI to 40 mL and clear volume infused.

19. Press RUN/HOLD key to start primary infusion.

20. Instrument will run approximately 360 seconds (6 minutes)

to complete delivery and then go into KVO mode. Stop

instrument within 1 second of entering KVO mode.

21. Make a note of scale reading in grams.

22. Note expected volume, as identified on 80VCS set insert.

23. Do not remove 80VCS set from instrument until one of

following conclusions is determined:

• Instrument passes rate verification and calibration is

not needed.

• Rate calibration number was changed and instrument

now passes verification.

• Mechanism replacement is required.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

10 Getting Started

Alternative Rate Accuracy Qualification Test (Continued)

Check-In and Configuration (Continued)

24. Calculate gravimetric accuracy as follows:

Gravimetric Volume Accuracy Error Computation

Vcollected = volume in flask in grams

Vexpected = characterized volume printed on 80VCS set

insert

Step 1: A = Vcollected / Vexpected

Step 2: B = A x 100

Step 3: % Error (Round % Error to nearest tenth of a

percent.) = B – 100

25. Result should be 0.0 ±3%.

26. If volume accuracy does not fall within required range of

±3.0% from expected volume and test results were:

• inside a range of -5.5% to +7.0% from expected

volume,

perform rate calibration (reference Technical Service

Manual). Set rate calibration number to 0.0% before

running rate test, to determine a new calibration

number.

• outside a range of -5.5% to +7.0% from expected

volume,

return instrument to Cardinal Health for repair or

replace mechanism.

27. Empty flask and reset scale to zero, in preparation for next

test.

NOTE:

À The factory default for the Monitoring Options mode is

Pressure.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

Check-In and Configuration (Continued)

Functional Test

1. Turn instrument on without set installed. Verify it beeps

and red alarm light flashes but does not stay lit.

2. Set infusion rate to 460 mL/h and VTBI to 100 mL.

3. With latch closed, press RUN/HOLD key and rate and

VTBI ≠ 0 to cause Set Out and Air In Line messages.

4. Open latch.

5. Install primed administration set with latch open.

6. Verify instrument displays Air In Line and Latch Open

messages.

7. Close latch and verify display returns to setup page.

Set Sensor Check / Pressure Calibration Verification

1. Access DIAGNOSTICS MODE by pressing and holding

upper left soft key on power-up. Reference Technical

Service Manual, “Troubleshooting” chapter, for details or

contact Cardinal Health Technical Support. À

2. Advance to D6 page and choose Cal Pressure (both

Channel A and Channel B for dual channel instruments).

3. Verify both 0 mmHg and 500 mmHg readings indicate

Pass.

4. Install a standard set and close latch. Verify reading is

over 170, to confirm set sensor operation.

5. Remove standard set and verify Sensor = reading is in

-80 to +30 mmHg range without set installed, to verify

pressure calibration. Á

DIAGNOSTICS MODE

ID No. : 000000000

SW Rev.: 08.XX

PM Due : 52 weeks

page

AB OPTIONS

NOTES:

À “08.XX” in the illustrated display represents the current

software revision.

Á If the reading is out of range, reference the Technical Service

Manual, “Pressure Calibration” section, or contact Cardinal

Health Technical Support for assistance.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

12 Getting Started

Check-In and Configuration (Continued)

Functional Test (Continued)

8. Perform Upstream Occlusion Test, as follows:

a. Verify infusion rate is set to 460 mL/h.

b. With instrument on hold, or at start-up, verify primary

VTBI is set to greater than 100 mL.

c. Press RUN/HOLD key to begin infusion.

d. Clamp off IV line just above instrument (about

2 inches) to simulate an upstream occlusion.

e. Verify instrument stops running, alarms, and displays

OCCLUSION UPSTREAM within 60 seconds.

f. Press RUN/HOLD key to silence alarm and put

instrument on hold.

g. Release or open clamp and remove from tubing.

h. Press RUN/HOLD key to resume infusion. Alarm

should not reoccur.

9. Perform Downstream Occlusion Test, as follows:

a. Continue infusing (from step 8h).

b. Verify rate is set to 460 mL/h.

c. Clamp off IV line just below instrument (about

2 inches) to simulate a downstream occlusion.

d. Allow instrument to run until it alarms OCCLUSION

DOWNSTREAM. Verify this occurs within 60

seconds.

e. Press RUN/HOLD key to silence alarm and put

instrument on hold.

f. Release or open clamp and remove from tubing.

g. Press RUN/HOLD key to resume infusion. Alarm

should not reoccur.

h. Press RUN/HOLD key to stop infusion.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

Flow Stop Test

1. With an administration set primed and loaded in

instrument, turn power off.

2. With all tubing clamps open and fluid container 2 or more

feet above instrument, verify no fluid flows through set.

3. Open latch and remove set. Verify no fluid flows through

set.

Ground Current Leakage Test

Use a DNI Nevada Model 232D (or equivalent) to measure

the ground leakage current. Refer to the test equipment’s

operation manual for the proper setup and measurement

technique. Leakage current must be ≤100μA for normal and

reversed line polarity.

Ground Resistance Test

Use a DNI Nevada Model 232D (or equivalent) to measure the

ground resistance. Measure resistance from the AC power

plug ground pin to the screw for the power cord strap, or to

the screw for the battery cover on the chassis. Refer to the

test equipment’s operation manual for the proper setup and

measurement technique. Resistance must be ≤0.10Ω.

CAUTION

Do not connect the ground

resistance probe to the pressure

transducer.

Instrument Configuration

Instrument Configuration for the SE Pump with the Guardrails®

Suite MX is set for each profile using the Editor Software, the

PC-based authoring tool. The Data Set is then transferred to

the SE Pump by qualified personnel.

The SE Pump may be operated with or without the Guardrails®

Suite MX protection. When an approved Data Set is

transferred to the SE Pump by qualified personnel and the

Profiles feature is enabled (ON) in instrument configuration,

then Guardrails® Suite MX protection is available.

Instrument configuration is set by qualified personnel in the

Data Set or Configuration and Diagnostics modes. When

the Profiles feature is not enabled (Off), or when no Data

Set has been transferred to the SE Pump, Guardrails® Suite

MX protection is not available (see "Primary Infusion – NO

Guardrails® Suite MX Protection" and "Secondary Infusion

- NO Guardrails® Suite MX Protection").

Check-In and Configuration (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

14 Getting Started

Administration Set Information

The SE Pump uses a wide variety of Flow Regulator

administration sets. The sets dedicated for use with the SE

Pump are designed for use with the instruments as well as

for gravity-flow stand-alone use. The unique, patented Flow

Regulator has an integral flow control device that minimizes

the risk of unintended flow when the set is removed from the

instrument, and provides accurate rate control during gravity

administration.

• For specific administration set instructions, reference

directions for use provided with set.

• Use aseptic technique when handling sets and syringes.

• Administration sets are supplied with a sterile and non-

pyrogenic fluid path for one time use. Do not re-sterilize

or re-use.

• For administration set replacement interval, refer to facility

protocol and/or government standards (such as: CDC

guidelines in the United States) and see "SmartSite®

Infusion Set" section of this Directions for Use (DFU).

• Discard administration set per facility protocol.

• For IV push medication (put instrument on hold), occlude

tubing above injection port during administration.

• Flush port(s) per facility protocol.

• Place a sterile replacement cap on open end of tubing

connector when not in use. Discard tubing when integrity

has been compromised.

General

SmartSite® Infusion Set

The Needle-Free Valve is designed to permit injection and

aspiration of fluids without the use of needles.

1. Use proper hand-hygiene procedures. Wash hands with

conventional antiseptic-containing soap and water or

disinfect with waterless alcohol-based gels or foams.

2. Prepare Needle-Free Valve.

• Always swab top of valve port, prior to every access,

with sterile 70% isopropyl alcohol wipe and allow to

dry.À

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

Administration Set Information (Continued)

NOTES:

À For multiple syringes, swab prior to each syringe access.

Á For infusions of blood, blood products or lipid emulsions

replace every 24 hours.

SmartSite® Infusion Set (Continued)

• Replace every 72 hours or 100 activations, whichever

comes first. Á

Prepare the primary solution container in accordance with the

manufacturer’s directions for use.

Use only sets dedicated for use with SE Pump.

Preparing Solution Container and Set

Thumb Clamp

Click

Flow Regulator

WARNINGS

• Use only sets dedicated for

use with the SE Pump. The

use of any other set may cause

improper instrument operation,

resulting in an inaccurate fluid

delivery or other potential

hazard.

• Discard if packaging is not intact

or protector caps are unattached.

1. Slide Flow Regulator thumb clamp down until an audible

click verifies it is in fully closed position.

2. Spike solution container.

3. Fill drip chamber to 2/3 full. À

4. Invert Flow Regulator.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

16 Getting Started

Administration Set Information (Continued)

5. Slide Flow Regulator thumb clamp to open position to

slowly prime set.

6. Close Flow Regulator clamp when priming is complete, as

in Step 1. Verify no fluid is flowing.

7. A gravity flow rate may be adjusted with Flow Regulator

thumb clamp, if desired.

NOTE:

À Open the vent cap on the spike if the container requires

venting.

Slide up to open

for priming.

Slide down to

close for loading.

Loading Set

1. Slide Flow Regulator thumb clamp down until an audible

click verifies it is in fully closed position.

Thumb Clamp

Click

Flow Regulator

2. Using both hands, press top and bottom of Flow Regulator

into instrument until it snaps into place.

a. Verify 3 gray fingers (clamp arms) on each side of

pumping mechanism have engaged Flow Regulator.

b. Let go of set. A properly loaded set should stay in

instrument.

Preparing Solution Container and Set (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Getting Started

Administration Set Information (Continued)

WARNING

After set installation, verify no fluid

is flowing through the administration

set’s drip chamber, to avoid free-

flow.

3. Press firmly just below blue thumb clamp on Flow

Regulator with one hand while using other hand to close

latch fully to left.

• If resistance is met while closing latch, remove set,

verify Flow Regulator is fully closed and then reinstall

set.

• Verify thumb clamp has moved to open (up) position

prior to starting infusion.

CAUTION

Before operating instrument, verify

that administration set is free from

kinks and installed correctly in

instrument.

Loading Set (Continued)

4. Attach set to patient’s vascular access device.

5. Verify flow from IV container after starting infusion.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

18 Getting Started

Removing Set

1. Place channel on hold.

2. Open latch.

• Flow Regulator automatically closes to prevent

accidental unintended flow.

Administration Set Information (Continued)

3. Press latch fully to right.

• Set is ejected from instrument.

WARNING

Even though the instrument

automatically closes the Flow

Regulator, verify the Flow

Regulator is closed when the set

is removed from the instrument to

prevent unintended flow.

CAUTION

Do not attempt to force the set

from the instrument. Send the

instrument to qualified service

personnel.

Changing Solution Container

1. Place channel on hold.

2. Remove empty solution container.

3. Spike new container.

4. Ensure drip chamber is filled to 2/3 full.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

References throughout this procedure to specific drugs and

drug doses are for illustration purposes only. Refer to specific

drug product labeling for information concerning appropriate

administration techniques and dosages.

Programming and Navigation Tips

Soft Keys

Soft Keys are the keys located on the left side and the bottom

of the main LCD display. They serve a variety of functions, as

indicated by the text in the display at the time. A soft key is

active if there is a tick mark (y) next to the key.

If there is no tick mark next to the key, then it is not active

and cannot be selected. [In the illustrated example Conc

(concentration) is not active.] Pressing an inactive key results

in an invalid keypress tone. Rate = 56.0 mL/h

Dose= 0.8 mg/kg/h

Conc= 100 mg/ 100 mL

Wt= 70 kg

AB OPTIONS

Entering Values

To enter programming values, select the desired parameter by

pressing the corresponding soft key. The field is highlighted.

To enter desired value, use the numeric keys then press the

ENTER key.

A value must be highlighted to be changed.

A flashing highlight indicates that the entry is incomplete.

Complete the entry and press the ENTER key.

To clear an existing value, press the CLEAR key. If the existing

value should not be cleared, pressing the CLEAR key a

second time (before pressing the ENTER key) restores that

value.

When all parameters required on a programming setup screen

have been entered, the ok soft key is used to confirm all

entries and continue programming.

Active Soft Keys

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

20 Programming

Programming and Navigation Tips (Continued)

Menus - With Guardrails® Suite MX Protection

MENU screens provide access to the Profile drug libraries and

to basic programming in both the primary and the secondary

mode: À

• MENU (Primary Main Menu)

• BOLUS MENU

• SECONDARY MENU

Press menu soft key while in primary programming mode to

display MENU.

OPTIONS

New Guardrails Fluid

Basic Infusion

New Guardrails Drug A

OPTIONS

BOLUS MENU

Repeat Last Bolus

New Bolus

Quit Bolus

OPTIONS

SECONDARY MENU

Basic SEC

Return to PRI

Guardrails SEC Drug A

Press menu soft key while in bolus programming mode to

display BOLUS MENU.

NOTE:

À When the Profiles feature is not enabled (Off), or when no

Data Set has been transferred to the SE Pump, Guardrails®

Suite MX protection is not available and these menus do not

appear.

Press menu soft key while in secondary programming mode to

display SECONDARY MENU.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Split Screen (Dual Channel Only)

When both channels are infusing, a split screen showing

programmed information for both channels displays

automatically after one minute.

Press A B key to switch immediately to split screen.

Press

O or

O key to stop split screen.

AB OPTIONS

mcg/kg/min

DOPamine

VI = 0.5

Fluid

Rate = 75.0

0.9% NS

VI = 40.9

Programming and Navigation Tips (Continued)

Menus - NO Guardrails® Suite MX Protection

MENU screens for optional modes can be accessed using the

OPTIONS key:

• MULTI-STEP MENU

• MULTI-DOSE MENU

• DOSE RATE MENU

CAUTION

Guardrails® Suite MX protection is

not available within the MULTI-STEP,

MULTI-DOSE OR DOSE-RATE

MENU options.

Powering On and Off

1. To turn channel on, press channel's POWER key.

• Instrument performs a self test when first channel is

powered on.

• All indicators and displays momentarily light.

• An audio tone sounds.

• Hold indicator flashes.

WARNING

Each time the instrument is

turned on verify and/or set the

monitoring mode, resistance alert

and/or pressure alarm limit. If the

monitoring mode, resistance alert

and/or pressure alarm limit are not

verified, the instrument may not be

operating with the desired occlusion

detection parameter(s).

OPTIONS

SEC

PRI

POWER

RUN

HOLD

PRI SEC HLD OPT

HLD PRI SECKVO OPT

POWER

RUN

HOLD

A B

ml/hr ml

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

22 Programming

Programming and Navigation Tips (Continued)

• System startup page displays briefly (08.XX in

example display represents current software

revision; ID No. is instrument serial number).

OPTIONS

Cardinal Health

SW Rev. : 08.xx

ID No. : - - - - - - - - -

• When self test completes, if Guardrails® Suite MX

protection is available, current profile screen appears. OPTIONS

Current Profile Is

Adult ICU

Hospital Name

DataSet ID 123456789

Accept Change

2. To power off, press and hold POWER key until display

turns off.

• If Profiles feature is not enabled, then NEW PATIENT?

screen appears.

AB OPTIONS

NEW PATIENT ?

"Yes" Clears Previous

Patient Data

no yes

Powering On and Off (Continued)

CAUTIONS

• Appearance of lines and/or dots

that remain on constantly when

the instrument is powered on may

indicate improper functioning of

the Main Display. Although the

instrument is functioning, return it

to qualified service personnel.

• Inspect LCD for anomalies

(improperly lit/unlit pixels).

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Programming and Navigation Tips (Continued)

Responding to Maintenance Reminder

If the Preventive Maintenance Reminder option is enabled and

the device is due for preventive maintenance a Maintenance

Reminder message appears at power up.

1. Notify appropriate facility personnel if a Maintenance

Reminder message appears.

2. If necessary, press continue soft key to temporarily

bypass reminder.

AB OPTIONS

continue

Maintenace

Reminder

Responding to Time Set Reminder

Following certain battery depleted conditions it is necessary to

re-set the internal clock so that CQI Reporter data integrity is

maintained. In such cases, a Verify Time reminder message

appears at power up.

1. Press Change soft key.

• Time set screen displays.

2. Press soft key next to parameter to be changed.

• Current value is highlighted.

3. To enter a new value, use numeric keypad, then press

ENTER key.

4. Verify that all fields are correct then press ok soft key to

continue programming.

OPTIONS

Accept Change

Skip

Verify Date / Time

Feb 28 2006

16:43

Month

OPTIONS

Day

Year

Time

2006

16h 43min

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

24 Programming

Guardrails® Suite MX Prompts

Soft Limits

Hard Limits

If programmed parameter is outside the Hard Limit for that care

area, a prompt appears indicating a value within range must be

entered before programming can continue.

Use numeric keys to enter a new value, then press ENTER

key.

AB OPTIONS

DOPAmine

Exceeds Hard Limit:

50 mcg/kg/min

REPROGRAM

Rate = 600.0 mL/h

Guardrails® Suite MX software allows the facility to create

Soft and/or Hard Limits for Guardrails® continuous dose,

Concentration, Guardrails® Bolus Dose, Bolus Dose

Administration Rate, Guardrails® intermittent total dose,

Intermittent Time, and IV Fluid Rate.

Within each profile the facility may also pre-define the following

Hard Limits: maximum patient weight (kg), maximum patient

body surface area (m2) and maximum rate (mL/h).

Additional prompts are provided if Time or VTBI are edited

resulting in a rate change, or if a VTBI significantly larger or

smaller than the bag volume is entered.

AB OPTIONS

no yes

override?

alteplase

Exceeds Soft Limit:

0.81 mg/kg/h

Override Dose Limit?

If programmed parameter is outside Soft Limit for that care area,

a prompt appears before programming can continue.

1. If it is inappropriate to override Soft Limit, press no soft key.

• Drug set up page displays.

2. Use numeric keys to enter a new value, then press ENTER

key.

3. If it is clinically appropriate and necessary to override

Soft Limit, press yes soft key.

• Programming may continue.

When a maximum dose limit is exceeded, ↑↑↑ precedes the drug

or fluid name. This indicates that the drug is infusing at a rate

exceeding the defined maximum limit for that profile.

When a minimum dose limit is exceeded, ↓↓↓ precedes the drug

or fluid name. This indicates that the drug is infusing at a rate

less than the defined minimum limit for that profile.

WARNING

Prior to overriding a Soft Limit

prompt, confirm the infusion

parameters are correct.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - With Guardrails® Suite MX Protection

1. To change Profile, press change soft key.

• Profile selection menu displays.

Adult ICU

AB OPTIONS

Cardiac Care Unit

Labor and Delivery

Medical / Surgical

page

2. To view additional Profile selections, press page soft key.

3. Press soft key next to desired new Profile.

• Confirm Profile screen appears.

CAUTION

If the correct profile is not

selected, the instrument may not

operate within the appropriate dosing

limits and operating parameters.

OPTIONS

Current Profile Is

Oncology

Hospital Name

DataSet ID 123456789

Accept Change

Selecting New Patient and Profile Options

Previous programming parameters may either be cleared or

preserved.

Cleared, if:

• Profile is changed.

• Profile is accepted but New Patient? - yes is selected.

Preserved, only if:

• Current Profile is accepted and New Patient? - no is

selected.

Changing Profile

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

26 Programming

OPTIONS

New Guardrails Fluid

Basic Infusion

New Guardrails Drug A

Once confirmed:

• Abbreviated Profile name appears in lower display.

• All previous programming parameters are cleared.

• MENU screen displays.

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

To retain currently active Profile, press Accept soft key.

• NEW PATIENT? screen displays.

OPTIONS

Current Profile Is

Oncology

Hospital Name

DataSet ID 123456789

Accept Change

To indicate programming is for a new patient and clear all

stored patient parameters from memory, press yes soft key.

• All previous patient data clears and there is no option to

Resume Previous Drug or Resume Previous Fluid.

• MENU screen displays.

NEW PATIENT?

“Yes” Clears Previous

Patient Data

AB OPTIONS

yes

Confirm Profile

Adult ICU

return

ABOPTIONS

4. To confirm Profile selection, press ok soft key.

To select another Profile, press return soft key.

Selecting New Patient and Profile Options (Continued)

Changing Profile (Continued)

Accepting Profile

Selecting New Patient Option

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - With Guardrails® Suite MX Protection

The following procedures are to be used only when the drug

to be infused is listed in the Drug Library. To access the Drug

Library, a hospital-defined best-practice Data Set must be

transferred using the Editor Software and the Profiles feature

must be enabled.

Continuous Infusion

When using a drug listed in the Drug Library, the drug

parameters are automatically calculated based on:

• drug and concentration selected

• weight entry (if required)

• rate or dose entry

1. Press New Guardrails Drug soft key.

• If 15 or less drugs are available in selected profile, a

list of drug names displays; otherwise, an alphabetic

preselection menu displays.

OPTIONS

New Guardrails Fluid

Basic Infusion

New Guardrails Drug A

Selecting New Patient and Profile Options (Continued)

Selecting New Patient Option (Continued)

To confirm programming is for same patient and retain all

stored patient parameters, press no soft key.

• All previous patient data is maintained.

• MENU screen displays.

• If last infusion on that channel was a Drug Library

entry, Resume Previous Drug appears as a MENU

selection.

• If last infusion on that channel was an IV Fluid,

Resume Previous Fluid appears as a MENU

selection.

• If last infusion on that channel was an optional mode

or a Basic Infusion, Return to ….? appears as a

MENU selection.

Primary Infusion Introduction

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

28 Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Continuous Infusion (Continued)

acyclovir

AB OPTIONS

albumin 25%

albumin 5%

alteplase

page

DOPamine

return

AB OPTIONS

400 mg / 250 mL

800 mg / 250 mL

- - - - mg / - - - - mL

alteplase

Stroke

return

OPTIONS

Dose in?

return

AB OPTIONS

Un/h

Un/kg/h

2. To use pre-selection menu press soft key corresponding

to first letter of desired drug. Select Drug A - F

AB OPTIONS

Select DrugG-M

Select DrugN-S

Select Drug T - Z

3. Press soft key next to desired drug name to select it.

• page soft key(s) may be used to view additional

selections.

• If applicable, an optional hospital-defined therapy

or clinical indication for delivery of this infusion may

appear (as in illustrated example, which reflects use

of alteplase). Different limits can be defined for same

drug with different therapeutic indications.

• If applicable, a weight-based or non-weight-based

option for delivery of this infusion may appear (as in

illustrated example which reflects use of heparin).

• If applicable, multiple concentration listings for delivery

of this infusion may appear (as in illustrated example

which reflects use of dopamine).

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Continuous Infusion (Continued)

4. Press soft key next to desired selection.

5. To confirm selection and continue programming, press ok

soft key.

• If a different selection is desired, press return soft

key to return to the drug list or press menu soft key

to return to MENU screen, then navigate to desired

selection and press ok soft key.

OPTIONS

ADVISORY

This Dosing Is For

Acute Ischemic

STROKE

alteplase

100 mg/100 mL

Dose in mg/kg/h

menu return ok

ABOPTIONS

stroke

AB OPTIONS

BolusOnly

Rate = - - - - - mL/h

Dose= - - - - - mg/kg/h

Conc= 100 mg/ 100 mL

Wt= - - - - - kg

6. If facility has defined a Clinical Advisory for selected drug,

a message appears. To indicate that information has

been noted and continue programming, press ok soft key.

• Infusion setup page displays.

7. An optional hospital-defined and editable starting value for

continuous infusion dose may already be entered.

To enter a value, use numeric data entry keys then press

ENTER key.

• Dose field is highlighted for first entry, but soft keys

can be used to highlight other parameters for entry

prior to dose. To automatically calculate dose

instead of rate, press Rate soft key and enter a rate

value. Once all entries have been completed, dose is

automatically calculated.

• If a drug with a defined standard concentration was

selected, Conc (concentration values, drug amount

and diluent volume) are automatically entered. (Notice

that these values are not editable).

• If a drug with -- / -- mL was selected, Conc

(concentration values of drug amount and diluent

volume), needs to be entered.

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

30 Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Continuous Infusion (Continued)

AB OPTIONS

VTBI= 0.0 mL

VI= 0.0 mL

alteplase

Bolus

AB OPTIONS

Rate = 56.0mL/h

Dose= 0.8 mg/kg/h

Conc= 100 mg/ 100 mL

Wt= 70 kg

OPTIONS

VTBI= 100.0 mL

VI=

alteplase

Bolus

mL0.0

• If selected drug is weight-based, Wt (patient weight in

kg) needs to be entered.

• If selected drug is not weight-based, Wt field does not

appear.

8. Verify that all parameters are correct and press ok soft

key to confirm.

• VTBI and VI setup page displays.

• VTBI field is highlighted.

9. To enter desired VTBI, use numeric keys then press

ENTER key.

• VI field is highlighted.

10. If there is a VI value that needs to be cleared, press

CLEAR key or press 0 (zero) key then press ENTER key.

11. To continue programming, press ok soft key.

• RUN/HOLD page displays.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

12. Verify that all parameters are correct, then press run soft

key or RUN/HOLD key to start infusion

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Continuous Infusion (Continued)

Pausing and Restarting Infusion

1. An infusion may be paused temporarily by pressing

channel RUN/HOLD key.

• Rate LED flashes while infusion is on hold.

• After 2 minutes, “Hold Time Exceeded” visual and

audio prompts begin. An additional 2 minute period

may be initiated by pressing either hold soft key or

channel RUN/HOLD key.

2. To restart infusion while on hold, press channel RUN/

HOLD key.

OPTIONS

Stroke

Rate = 56.0 mL/h A

Conc = 100 mg/100 mL

Wt = 70 kg

Adult ICU

OPTIONS

Dose = 0.8 mg/kg/h

VTBI = 100.0 VI = 0.0

Rate = 56.0 mL/h A

run

menu setup

alteplase

13. To briefly view setup parameters (therapy, concentration,

patient weight, current profile) from RUN/HOLD page or

during a running infusion, press 4 soft key.

Making Changes During Continuous Infusion

Continuous infusion parameters (Rate, Dose or VTBI) may be

changed without pausing the infusion and VI may be cleared.

1. Select

O or

O key, as necessary.

2. Press soft key next to parameter to be edited.

• Current value is highlighted.

Making Changes to Rate, Dose or VTBI

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

32 Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Making Changes to Concentration or

Patient Weight

Infusion must be paused before making changes. If a drug

with a defined standard concentration was selected, Conc

(concentration) values are not editable.

1. To pause infusion, press channel's RUN/HOLD key.

2. Press set up soft key.

3. Press soft key next to parameter to be edited.

• Current value is highlighted.

4. To enter a new value, use numeric keypad then press

ENTER key.

Resuming Interrupted Infusion

If a channel has been powered off during an infusion, previous

programming may be resumed if:

• One channel of a dual channel device remained on.

• Current profile is accepted and New Patient? – no is

selected during start up (see "Selecting New Patient and

Profile Options").

1. Select desired channel as necessary.

Making Changes During Continuous Infusion (Continued)

Making Changes to Rate, Dose or VTBI

(Continued)

3. Make changes:

a. To enter a new value, use numeric keypad.

b. To reset Volume Infused to 0.0 mL, press CLEAR or

0 (zero) key.

4. To accept new value, press ENTER key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

OPTIONS

New Guardrails Fluid

Resume Previous Drug

New Guardrails Drug A

Basic Infusion

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

3. Press ok soft key to confirm drug, therapy, concentration

and dosing units.

4. If facility has defined a Clinical Advisory for selected drug,

a message appears. To indicate that information has

been noted and continue programming, press ok soft key.

• Previous infusion setup page appears.

5. Verify parameters are correct. If a change is required, see

“Making Changes During Continuous Infusion”.

6. Press ok soft key to continue.

• RUN/HOLD page displays.

7. Verify that all parameters are correct, then press run soft

key or RUN/HOLD key to start infusion.

2. Press Resume Previous Drug soft key.

• Previous drug review screen displays.

Resuming Interrupted Infusion (Continued)

When the primary VTBI reaches 0.0mL, the instrument

automatically switches to the configured KVO (keep vein open)

rate, or remains at the current infusion rate, whichever is less.

• KVO rate flashes in rate LED display.

• Programmed infusion rate continues to display in Main

Display.

• KVO flashes in infusion status bar.

• KVO alert tone sounds (may be silenced for 2 minutes

using Silence key).

• VTBI = 0 (INFUSION IN KVO in Models 7131/7231)

message flashes in Main Display.

OPTIONS

Dose = 0.8 mg/kg/h

VTBI = 0.0 VI = 100.0

Rate = 56.0 mL/h A

Channel A

VTBI = 0

KVO Mode

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

34 Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Resuming Operation from KVO Mode

1. To place channel on hold, press RUN/HOLD key.

2. Press VTBI soft key.

• VTBI is highlighted.

3. To enter desired VTBI, use numeric keys then press

ENTER key.

4. To resume infusion, press run soft key or RUN/HOLD key.

Clearing Volume Infused

The volume infused counter increments as ﬂ uids are infused

through a given channel. All ﬂ uids infused in primary mode,

including boluses, all ﬂ uids infused in secondary mode and all

ﬂ uids infused in KVO mode are counted.

1. To reset volume infused counter to 0.0mL, press VI soft

key.

• VI field is highlighted.

2. Press CLEAR key or press 0 (zero) key then press

ENTER key.

Bolus Dose

A Bolus Dose can be programmed at the beginning of, or

during a continuous infusion. The drug being programmed

must be a bolusable drug selected from the Drug Library, as

described in the following procedures.

Bolus volume must be at least 1 mL and not more than

999.9 mL. Programming a bolus dose that calculates a bolus

volume outside that range results in a message, "Bolus

VTBI Less than 1 mL Not Allowed" or "Bolus VTBI More than

999.9 mL Not Allowed".

Bolus dose parameters may not be edited during bolus

infusion. If new parameters are desired, select New Bolus

Dose from the Bolus menu.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Delivering a Bolus Dose Prior to Beginning

Continuous Infusion

1. Set up infusion as described in “Continuous Infusion”

procedure, steps 1 - 10. Do not start infusion.

2. On VTBI and VI setup page, press Bolus soft key.

• Bolus programming page displays.

• Bolus field is highlighted.

AB OPTIONS

VTBI= 100.0 mL

VI= 0.0 mL

alteplase

Bolus

3. An optional hospital-defined and editable starting value for

bolus dose may already be entered.

To enter a value, use numeric data entry keys then press

ENTER key.

• If bolus is weight-based and weight has already been

programmed in same channel, Wt (patient weight in

kg) is automatically entered.

• If bolus is weight-based and weight has not yet been

programmed in same channel, Wt (patient weight in

kg) needs to be entered.

• If bolus is not weight-based, Not Used displays in Wt

field.

4. An optional hospital-defined bolus dose administration

rate may have been used to calculate an editable Time in

minutes (1-99) to deliver programmed bolus dose.

To enter a Time value, use numeric data entry keys then

press ENTER key.

5. Verify parameters are correct and press ok soft key (see

"Guardrails® Suite MX Prompts").

• Bolus RUN/HOLD page displays.

OPTIONS

Wt = - - kg

Time = - - min

Alteplase Bolus

Bolus = - - - - mg/kg

Bolus = 0.09 mg/kg

OPTIONS

Wt = 70 kg

Time = 1 min

Alteplase Bolus

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

36 Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Delivering a Bolus Dose Prior to Beginning

Continuous Infusion (Continued)

6. Verify that all parameters are correct, then press run soft

key or RUN/HOLD key to start infusion.

• When bolus dose completes, an audio tone sounds

and “Bolus Dose Complete” briefly displays, and

infusion automatically transitions to continuous rate. Bolus = 0.09 mg/kg

OPTIONS

Wt = 70 kg

Time Left = 1 min

run

Alteplase Bolus

1. Press OPTIONS key.

2. Press Bolus soft key.

• BOLUS MENU displays.

3. Press New Bolus soft key.

To repeat a previous bolus, press Repeat Last Bolus soft

key.

• Bolus Programming page displays.

• Bolus field is highlighted.

4. An optional hospital-defined and editable starting value for

bolus dose may already be entered.

To enter a value, use numeric data entry keys then press

ENTER key.

• If bolus is weight-based and weight has already been

programmed in same channel, Wt (patient weight in

kg) is automatically entered.

• If bolus is weight-based and weight has not yet been

programmed in same channel, Wt (patient weight in

kg) needs to be entered.

• If bolus is not weight-based, Not Used displays in Wt

field.

Delivering a Bolus Dose During a Continuous Infusion

OPTIONS

BOLUS MENU

Repeat Last Bolus

New Bolus

Quit Bolus

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Delivering a Bolus Dose During a Continuous Infusion

(Continued)

5. An optional hospital-defined bolus dose administration

rate may have been used to calculate an editable Time in

minutes to deliver programmed bolus dose.

To enter a value, use numeric data entry keys then press

ENTER key.

6. Verify parameters are correct and press ok soft key

to transition from continuous to bolus infusion (see

"Guardrails® Suite MX Prompts").

• When bolus dose completes, an audio tone sounds

and Bolus Dose Complete briefly displays, and

infusion automatically transitions back to continuous

rate.

OPTIONS

Dose = 0.9 mg/kg/h

Rate = 50.0 mL/h A

Channel A

Bolus Dose Complete

The Bolus Only feature is used to deliver single boluses from

a fluid container without delivering a continuous infusion. The

feature is not available once a continuous dose or rate has

been entered, or if an initial value for continuous infusion dose

has been entered in the Data Set.

1. Follow steps 1 - 6 in "Continuous Infusion". DO NOT enter

a dose or rate.

2. Press BolusOnly soft key.

• Bolus Programming page displays.

• Bolus field is highlighted.

3. An optional hospital-defined and editable starting value for

bolus dose may already be entered.

Bolus Only

AB OPTIONS

BolusOnly

Rate = - - - - - mL/h

Dose= - - - - - mg/kg/h

Conc= 100 mg/ 100 mL

Wt= - - - - - kg

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

38 Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Bolus Only (Continued)

To enter a value, use numeric data entry keys then press

ENTER key.

• If bolus is weight-based and weight has already been

programmed in same channel, Wt (patient weight in

kg) is automatically entered.

• If bolus is weight-based and weight has not yet been

programmed in same channel, Wt (patient weight in

kg) needs to be entered.

• If bolus is not weight-based, Not Used displays in Wt

field.

4. An optional hospital-defined bolus dose administration

rate may have been used to calculate an editable Time in

minutes (1-99) to deliver programmed bolus dose.

To enter a time value, use numeric data entry keys then

press ENTER key.

5. Verify parameters are correct and press ok soft key (see

"Guardrails® Suite MX Prompts").

• Bolus Only bag volume confirmation page displays.

6. Verify that bag contains an adequate volume to deliver

programmed dose as specified and press ok soft key.

• Bolus RUN/HOLD page displays.

AB OPTIONS

Bolus Only

Make Sure Bag

Contains At Least

6.3 mL

return

OPTIONS

Bolus Dose Complete A

7. Verify that all parameters are correct and press run soft

key or RUN/HOLD key to start infusion.

• When bolus dose completes, an audio tone sounds

and Bolus Dose Complete displays until user takes

action.

• No continuous infusion or KVO rate occurs.

• Dashes “----“ appear in Rate LED display.

• No alarm occurs.

8. Press menu key to return to Bolus Menu.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Stopping Bolus Dose

1. To place channel on hold, press channel RUN/HOLD key.

2. Press menu soft key.

• Bolus Menu displays.

3. Press Quit Bolus soft key.

4. To start continuous infusion, if one was programmed,

verify parameters are correct and then press run soft key

or channel RUN/HOLD key.

Repeating a Bolus Dose

A bolus dose that has completed may be repeated. If a bolus

dose was stopped prior to completion the Repeat Bolus Dose

soft key becomes inactive.

1. Press Options key.

2. Press Bolus soft key.

• Bolus Menu displays.

3. Press Repeat Last Bolus soft key.

• Bolus Programming page displays.

4. To accept current bolus dose and time values and begin

bolus delivery, press ok soft key.

To edit bolus or time, select desired field, use numeric

data entry keys to enter a new value, then press ENTER

key and press ok soft key to begin bolus delivery.

• When bolus dose completes, an audio tone sounds,

Bolus Dose Complete briefly displays, and infusion

automatically transitions to continuous rate if one was

programmed.

• If no continuous rate or dose was programmed an

audio tone sounds and Bolus Dose Complete

displays until user takes action (see "Bolus Only").

OPTIONS

BOLUS MENU

Repeat Last Bolus

New Bolus

Quit Bolus

OPTIONS

BOLUS MENU

Repeat Last Bolus

New Bolus

Quit Bolus

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

40 Programming

Intermittent Infusion

When using a drug listed in the Drug Library, the drug

parameters are automatically calculated based on:

• drug amount

• weight entry or BSA entry (if required)

• VTBI entry

• time or rate entry

1. Press New Guardrails Drug soft key.

• If 15 or less drugs are available in selected profile, a

list of drug names displays; otherwise, an alphabetic

pre-selection menu displays.

OPTIONS

New Guardrails Fluid

Basic Infusion

New Guardrails Drug A

2. To use pre-selection menu press soft key corresponding

to first letter of desired drug. Select Drug A - F

AB OPTIONS

Select DrugG-M

Select DrugN-S

Select Drug T - Z

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

octreotide

OPTIONS

paclitaxel

pentostatin

potassium CHLORIDE

page

3. Press soft key next to desired drug name to select it.

• page soft key(s) may be used to view additional

selections.

• If applicable, an optional hospital-defined therapy

or clinical indication for delivery of this infusion may

appear (as in illustrated example, which reflects use

of paclitaxel). Different limits can be defined for same

drug with different therapeutic indications.

paclitaxel

every three weeks

weekly

return

ABOPTIONS

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

VANCOmycin

return

AB OPTIONS

1000 mg / 200 mL

1000 mg / 250 mL

- - - - mg / - - - - mL

• If applicable, a weight-based, non-weight-based or

BSA-based option for delivery of this infusion may

appear.

• If applicable, multiple concentration listings for delivery

of this infusion may appear (as in illustrated example

which reflects use of vancomycin).

4. Press soft key next to desired selection.

5. To confirm selection and continue programming, press ok

soft key.

• If a different selection is desired, press return soft key

to return to drug list or press menu soft key to return to

MENU screen, then navigate to desired selection and

press ok soft key.

Intermittent Infusion (Continued)

paclitaxel

every three weeks

Dose in mg/m

OPTIONS

okreturn

6. If facility has defined a Clinical Advisory for selected drug,

a message appears. To indicate that information has

been noted and continue programming, press ok soft key.

• Intermittent infusion setup page displays.

OPTIONS

Steroid Premeds

Non-PVC tubing

Filter Required

ADVISORY ok

7. Enter parameters as needed.

• If a drug with a defined standard concentration was

selected, Conc (concentration values, drug amount

and diluent volume) are automatically entered. (Note

that these values are not editable).

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

42 Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Intermittent Infusion (Continued)

Conc = 280 mg/ 500 mL

BSA = 1.6 m2

Dose =175 mg/m2

AB OPTIONS

paclitaxel

OPTIONS

Time=3h0min

Rate = 166.7 mL/h A

paclitaxel

rate - time

VTBI= VI = 0.0 mL500.0 mL

AB OPTIONS

paclitaxel

Conc = - - - - mg/ - - - - mL

BSA = - - - - m2

Dose = - - - - - mg/m2

• If a drug with -- / -- mL was selected, Conc

(concentration values, drug amount and diluent

volume), need to be entered. Drug amount is total

dose of drug in fluid container. Diluent Volume is total

volume of fluid container.

• If selected drug is weight-based, Wt (patient weight in

kg) needs to be entered.

• If selected drug is BSA-based, BSA (body surface

area in meters squared) needs to be entered.

• If selected drug is not weight-based or BSA-based, Wt

or BSA field does not appear.

• Once all required parameters have been entered, total

calculated dose displays. This value is not editable.

8. Verify that all parameters are correct and press ok soft

key to confirm (see "Guardrails® Suite MX Prompts”).

• Rate/VTBI/Time page displays.

• VTBI value is highlighted.

• An editable value derived from diluent volume is

automatically entered.

9. To accept value, press ENTER key.

To enter another value, use numeric data entry keys then

press ENTER key.

• The VI field is highlighted.

10. If there is a VI value that needs to be cleared, press

CLEAR key or press 0 (zero) key then press ENTER key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Intermittent infusions must be paused to change parameters

(Rate, VTBI or Time) or to clear VI.

1. Press RUN/HOLD key for desired channel.

2. Press soft key next to parameter to be edited.

• Current value is highlighted.

3. Make changes:

a. To enter a new value, use numeric keypad.

b. To reset volume infused to 0.0 mL, press CLEAR or 0

(zero) key.

4. To accept new value, press ENTER key.

• Rate can be entered to calculate time or if time entry

is desired, press rate - time soft key. It changes to

rate - time , indicating that time may be entered.

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

Intermittent Infusion (Continued)

11. An optional hospital-defined and editable starting value for

time may already be entered.

To enter a value, use numeric data entry keys to enter

hours (0-99), then minutes (0-59). Press ENTER key to

accept each entry.

• Time can be entered to calculate rate or if rate entry

is desired, press rate - time soft key. It changes to

rate - time, indicating that rate may be entered.

12. Verify that all parameters are correct and press ok soft

key (see "Guardrails® Suite MX Prompts”).

• RUN/HOLD page displays.

13. Verify that all parameters are correct and press run soft

key or RUN/HOLD key to start infusion.

14. To briefly view setup parameters (therapy, total dose,

concentration, patient weight or BSA, current profile) from

RUN/HOLD page or during a running infusion, press 4

soft key.

Making Changes During Intermittent Infusion

OPTIONS

VTBI = 500.0 mL VI = 0.0 mL

Time = 3 h 0 min

Rate = 166.7 mL/h A

run

menu rate - time

paclitaxel

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

44 Programming

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

IV Fluid Infusion

1. Press New Guardrails Fluid soft key.

• If 15 or less fluids are available in selected profile, a

list of fluid names displays; otherwise, an alphabetic

pre-selection menu displays.

2. To use pre-selection menu press soft key corresponding

to first letter of desired fluid.

OPTIONS

TPN

page

3. Press soft key next to desired fluid name to select it.

• page soft key(s) may be used to view additional

selections.

• If applicable, an optional hospital-defined therapy

or clinical indication for delivery of this infusion may

appear. Different rate limits can be defined for same

fluid with different therapeutic indications.

4. Press soft key next to desired selection.

5. To confirm selection and continue programming, press ok

soft key.

• If a different selection is desired, press return soft key

to return to fluid list or press menu soft key to return to

MENU screen, then navigate to desired selection and

press ok soft key.

OPTIONS

New Guardrails Fluid

Basic Infusion

New Guardrails Drug A

Select Fluid A - F

AB OPTIONS

Select Fluid G-M

Select Fluid N-S

Select Fluid T - Z

Confirm fluid

TPN

ABOPTIONS

ok return

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

6. If a Clinical Advisory has been defined for selected fluid, a

message appears. To indicate that information has been

noted and continue programming, press ok soft key.

Primary Infusion - With Guardrails® Suite MX Protection (Continued)

IV Fluid Infusion (Continued)

• IV Fluid setup page displays.

• Rate field is highlighted.

OPTIONS

VTBI = 0.0 mL

VI = 0.0 mL

TPN

Rate = - - - - - mL/h

7. To enter a value, use numeric data entry keys then press

ENTER key (see "Guardrails® Suite MX Prompts”).

• VTBI field is highlighted.

8. To enter a VTBI value, use numeric data entry keys then

press ENTER key.

• VI field is highlighted.

9. If there is a VI value that needs to be cleared, press

CLEAR key or press 0 (zero) key then press ENTER key.

10. Verify that all parameters are correct and press run soft

key or RUN/HOLD key to start infusion. Rate = 83.3 mL/h

OPTIONS

VTBI = 2000.0 mL

VI = 0.0 mL

TPN

run

AB OPTIONS

ADVISORY

0.22 micron filter

Dedicated Line

11. To briefly view current profile from RUN/HOLD page or

during a running infusion, press 4 soft key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

46 Programming

Secondary Infusion - With Guardrails® Suite MX Protection

Introduction

This mode is designed to support automatic secondary

infusions (“piggybacking”) in the same channel. A secondary

infusion can be programmed as a Basic SEC or Guardrails

SEC drug. When the secondary VTBI reaches zero, an audio

tone sounds (if enabled), Secondary Complete message

displays briefly, and the primary infusion rate automatically

resumes.

When the instrument is programmed and delivering in the

secondary mode, the primary infusion is temporarily stopped

and fluid is drawn from the secondary container. Delivery

from the primary container resumes when the fluid level in the

secondary line is level with the fluid in the primary container.

Primary infusion must be on hold to program secondary

infusion.

A secondary infusion may be programmed only after a primary

IV Fluid (that supports secondary mode) or a primary Basic

Infusion has been programmed.

A list of IV Fluid entries is created in the Data Set that is

developed and approved by the facility’s own multidisciplinary

team using the Editor Software, the PC-based authoring tool.

Each entry is determined to be either appropriate to support

secondary infusions or not. The secondary key is unavailable

for selections that have been designated as inappropriate for

secondary delivery. Pressing the SEC key after programming

a fluid that does not support secondary infusions results in a

message, “Secondary not allowed with this fluid”.

The maximum rate for a secondary infusion is 600 mL/h.

For information regarding flow sensor use with secondary

infusions, see "General Information", "Flow Sensor".

WARNINGS

• Secondary applications require

the use of a check valve set on

the primary IV line.

• The secondary solution

container must be higher than

the primary solution container.

• The secondary VTBI settings

require consideration of

variables; such as, factory

overfill, medication additions.

Underestimating the volume

causes the remaining secondary

solution to be infused at the

primary rate; overestimating

results in the primary solution

being infused at the secondary

rate. Multiple doses from a

single container are not possible.

• The clamp on the secondary

administration set must be

opened. If the clamp is not

opened, the fluid is delivered

from the primary container.

• The secondary administration

set must be primed prior

to beginning the secondary

infusion.

• Ensure proper setup of

secondary systems to make sure

of proper flow.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Setup

1. Open secondary administration set package, remove set

and close clamp.

2. Insert administration set spike into prepared fluid container

and hang secondary container, following accepted

hospital/facility procedure.

3. Fill drip chamber to 2/3 full.

4. Open secondary administration set clamp and prime set.

Close clamp.

5. Attach secondary administration set to upper injection site

on primary set.

6. Using hanger(s) provided with secondary administration

sets, lower primary fluid container until bottom of

secondary container is at least 9½” above fluid level in

primary container.

Secondary Infusion - With Guardrails® Suite MX Protection (Continued)

Hanger

Secondary Container

Primary Container

at least 9½”

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

48 Programming

Secondary Infusion - With Guardrails® Suite MX Protection (Continued)

When using a secondary intermittent drug listed in the Drug

Library, the drug parameters are automatically calculated

based on:

• drug amount

• weight entry or BSA entry (if required)

• VTBI entry

• time or rate entry

Primary infusion must be on hold to program secondary

infusion.

1. Press SEC key.

• Secondary Menu displays.

2. Press Guardrails SEC Drug soft key.

• If 15 or less drugs are available in secondary library

of selected profile, a list of drug names displays;

otherwise, an alphabetic pre-selection menu displays.

OPTIONS

SECONDARY MENU

Basic SEC

Return to PRI

Guardrails SEC Drug A

Tobramycin

AB OPTIONS

TOPOtecan

Trastuzumab

VANCOmycin

Select Drug A - F

AB OPTIONS

Select DrugG-M

Select DrugN-S

Select Drug T - Z

4. Press soft key next to desired drug name to select it.

3. To use pre-selection menu press soft key corresponding

to first letter of desired drug.

Secondary Intermittent Infusion

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Secondary Infusion - With Guardrails® Suite MX Protection (Continued)

Secondary Intermittent Infusion (Continued)

VANCOmycin

Central

Peripheral

return

ABOPTIONS

• If applicable, an optional hospital-defined therapy

or clinical indication for delivery of this infusion may

appear (as in illustrated example, which reflects use of

vancomycin). Different limits can be defined for same

drug with different therapeutic indications.

• If applicable, a weight-based, non-weight-based or

BSA-based option for delivery of this infusion may

appear (as in illustrated example, which reflects use of

acyclovir).

OPTIONS

acyclovir

mg/kg

return

mg/m 2

VANCOmycin

return

AB OPTIONS

500 mg / 100 mL

1000 mg / 200 mL

- - - - mg / - - - - mL

• If applicable, multiple concentration listings for delivery

of this infusion may appear (as in illustrated example

which reflects use of vancomycin).

5. Press soft key next to desired selection.

6. To confirm selection and continue programming, press ok

soft key.

• If a different selection is desired, press return soft key

to return to drug list or press menu soft key to return to

MENU screen, then navigate to desired selection and

press ok soft key.

7. If a Clinical Advisory has been defined for selected drug, a

message appears. To indicate that information has been

noted and continue programming, press ok soft key.

• Intermittent infusion setup page displays.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

50 Programming

Secondary Intermittent Infusion (Continued)

8. Enter parameters as needed.

• If a drug with a defined standard concentration was

selected, Conc (concentration values, drug amount

and diluent volume) are automatically entered. (Note

that these values are not editable).

• If a drug with -- / -- mL was selected, Conc

(concentration values, drug amount and diluent

volume), needs to be entered. Drug amount is total

dose of drug in fluid container. Diluent volume is total

volume of fluid container.

• If selected drug is weight-based, Wt (patient weight in

kg) needs to be entered.

• If selected drug is BSA-based, BSA (body surface

area in meters squared) needs to be entered.

• If selected drug is not weight-based or BSA-based, Wt

or BSA field does not appear.

• Once all required parameters have been entered, total

calculated dose displays. This value is not editable.

9. Verify that all parameters are correct and press ok soft

key to confirm (see "Guardrails® Suite MX Prompts”).

• Rate/VTBI/Time page displays.

• VTBI field is highlighted.

• An editable value derived from diluent volume is

automatically entered.

10. To accept value, press ENTER key.

To enter another value, use numeric data entry keys then

press ENTER key.

• VI field is highlighted.

11. If there is a VI value that needs to be cleared, press

CLEAR key or press 0 (zero) key then press ENTER key.

(This VI value includes all fluids infused on this channel in

Primary and Secondary mode since last cleared.)

Secondary Infusion - With Guardrails® Suite MX Protection (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

12. An optional hospital-defined and editable starting time for

Time may already be entered.

To enter a value, use numeric data entry keys to enter

hours (0-99), then minutes (0-59). Press ENTER key to

accept each entry.

• Time can be entered to calculate rate or if rate entry

is desired, press rate - time soft key. It changes to

rate - time, indicating that rate may be entered.

13. Verify that all parameters are correct and press ok soft

key (see "Guardrails® Suite MX Prompts”).

• A Secondary Clamp reminder message displays.

14. Verify that secondary clamp is open before proceeding,

then press yes soft key.

• RUN/HOLD page displays.

Secondary Intermittent Infusion (Continued)

Secondary Infusion - With Guardrails® Suite MX Protection (Continued)

AB OPTIONS

IS SECONDARY

CLAMP OPEN?

yes

15. Verify that all parameters are correct and press run soft

key or RUN/HOLD key to start infusion.

16. To briefly view setup parameters (therapy, total dose,

concentration, patient weight or BSA and current profile)

from RUN/HOLD page or during a running infusion, press

4 soft key.

• When secondary VTBI reaches 0.0mL:

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

52 Programming

Primary Infusion - NO Guardrails® Suite MX Protection

The following procedures should be used only when the

drug to be infused is not listed in the Drug Library or when

the Profile feature is set to OFF in the instrument system

configuration.

To indicate programming is for a new patient and clear all

stored patient parameters from memory, press yes soft key.

• All previous patient data clears.

To confirm programming is for same patient and retain all

stored patient parameters, press no soft key.

NEW PATIENT?

“Yes” Clears Previous

Patient Data

AB OPTIONS

yes

Selecting New Patient Option - Profiles Feature Not

Enabled (OFF)

Basic Infusion

If Guardrails® Suite MX protection is available and Basic

Infusion is desired, it can be accessed through the MENU.

If the Profile feature is set to OFF in the instrument

configuration, or no Data Set is loaded, the Basic Infusion

page displays by default.

1. Press Basic Infusion soft key.

• Basic Infusion RUN/HOLD page displays.

• Rate field is highlighted.

2. To accept current value, press ENTER key.

To enter desired value, use numeric data entry keys then

press ENTER key.

• VTBI field is highlighted.

3. To accept value, press ENTER key.

To enter another VTBI value, use numeric data entry keys

then press ENTER key.

• VI field is highlighted.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - NO Guardrails® Suite MX Protection (Continued)

4. If there is a VI value that needs to be cleared, press

CLEAR key or press 0 (zero) key then press ENTER key.

5. Verify that all parameters are correct and press run soft

key or RUN/HOLD key to start infusion.

6. To briefly view current profile from RUN/HOLD page or

during a running infusion, press 4 soft key.

Basic Infusion (Continued)

When the Profiles feature is set to OFF or when no Data Set

has been transferred to the SE Pump, Guardrails® Suite MX

protection is not available and this section does not apply.

A basic infusion may be promoted to a continuous drug

infusion or a fluid infusion with Guardrails® Suite MX protection

while infusing.

A basic infusion may not be promoted to an intermittent drug.

If an intermittent drug is selected a Pri Running message is

displayed.

Promoting Basic Infusion to

Guardrails® Suite MX Protection Infusion

Infusion must be running in the Basic Primary Mode.

1. Select desired channel as necessary.

2. Press Options key.

3. Press Guardrails Menu soft key.

4. Press New Guardrails Drug soft key.

5. To use pre-selection menu press soft key corresponding

to first letter of desired drug.

Promoting Basic Infusion to

Guardrails® Drug Infusion

Select Drug A - F

AB OPTIONS

Select DrugG-M

Select DrugN-S

Select Drug T - Z

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

54 Programming

Primary Infusion - NO Guardrails® Suite MX Protection (Continued)

OPTIONS

Alprostadil

Bretylium

Bumetanide

Diltiazem

page

7. To confirm selection and continue programming, press ok

soft key.

• If a different selection is desired, press return soft key

to return to drug list or press menu soft key to return to

MENU screen, then navigate to desired selection and

press ok soft key.

8. If a Clinical Advisory has been defined for selected drug, a

message appears. To indicate that information has been

noted and continue programming, press ok soft key.

• Dose field is highlighted.

9. An optional hospital-defined and editable starting value for

continuous infusion dose may already be entered.

To enter a value, use numeric data entry keys then press

ENTER key.

• Dose field is highlighted for first entry, but soft keys

can be used to highlight other parameters for entry

prior to dose. To automatically calculate dose

instead of rate, press rate soft key and enter a rate

value. Once all entries have been completed, dose is

automatically calculated.

• If a drug with a defined standard concentration was

selected, Conc (concentration values, drug amount

and diluent volume) is automatically entered. (Note

that these values are not editable).

• If a drug with -- / -- mL was selected, Conc

(concentration values, drug amount and diluent

volume), needs to be entered.

6. Press soft key next to desired drug name to select it.

• page soft key(s) may be used to view additional

selections.

Promoting Basic Infusion to

Guardrails® Drug Infusion (Continued)

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - NO Guardrails® Suite MX Protection (Continued)

Promoting Basic Infusion to

Guardrails® Drug Infusion (Continued)

• If selected drug is weight-based, Wt (patient weight in

kg) needs to be entered.

• If selected drug is not weight-based, Wt (patient

weight) field does not appear.

10. Verify that all parameters are correct and press ok soft

key to confirm.

Promoting Basic Infusion to

Guardrails® IV Fluid Infusion

Infusion must be running in the Basic Primary Mode.

1. Select desired channel as necessary.

2. Press Options key.

3. Press Guardrails Menu soft key.

4. Press New Guardrails Fluid soft key.

5. To use pre-selection menu press soft key corresponding

to first letter of desired fluid.

6. Press soft key next to desired fluid name to select it.

• page soft key(s) may be used to view additional

selections.

Select Fluid A - F

AB OPTIONS

Select Fluid G-M

Select Fluid N-S

Select Fluid T - Z

OPTIONS

1/2 NS

Blood (RBCs)

return page

D5 1/2 NS+KCL 10mEq/L

D5 1/2 NS

7. To confirm selection and continue programming, press ok

soft key.

• If a different selection is desired, press return soft key

to return to fluid list or press menu soft key to return to

MENU screen, then navigate to desired selection and

press ok soft key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

56 Programming

Primary Infusion - NO Guardrails® Suite MX Protection (Continued)

Promoting Basic Infusion to

Guardrails® IV Fluid Infusion (Continued)

8. If a Clinical Advisory has been defined for selected fluid, a

message appears. To indicate that information has been

noted and continue programming, press ok soft key.

• IV Fluid setup page displays.

• Rate field is highlighted and flashing indicating that

current value must be either approved or edited.

9. To accept current rate press ENTER key.

To enter a value, use numeric data entry keys then press

ENTER key.

Dose Rate Calculation-Drug? NO DOSE LIMIT - Profiles

Feature Enabled (ON)

The following procedures are to be used only when the drug to

be infused is NOT listed in the Drug Library.

When using Drug? – NO DOSE LIMIT, drug parameters are

automatically calculated based on:

• concentration

• weight entry (if required)

• rate or dose entry

1. Press New Guardrails Drug soft key.

• If 15 or less drugs are available in selected profile, a

list of drug names displays; otherwise, an alphabetic

pre-selection menu displays.

OPTIONS

Primary Infusion

New Guardrails Drug

Resume Previous Drug

2. To use pre-selection menu press T – Z soft key, press

page soft key to go to end of drug list, then press Drug?

– NO DOSE LIMIT soft key.

Select Drug A - F

AB OPTIONS

Select DrugG-M

Select DrugN-S

Select Drug T - Z

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - NO Guardrails® Suite MX Protection (Continued)

AB OPTIONS

Drug? NO DOSE LIMIT

page

Press 0 (zero) numeric key then press Drug? – NO DOSE

LIMIT soft key.

• Dosing unit in dose/weight/time displays with dose

segment highlighted.

Dose Rate Calculation-Drug? NO DOSE LIMIT - Profiles

Feature Enabled (ON) (Continued)

3. To scroll through units available, press and release

soft key. When correct unit is displayed, press ENTER

key.

• If weight-based dosing is desired, press ENTER to

advance to time segment

If non-weight-based dosing is desired, press soft

key to clear segment, then press ENTER (weight field

disappears).

• If time unit is appropriate, press ENTER to advance to

concentration field.

Press soft key to scroll through available time unit

choices. Press ENTER when correct unit displays.

• If concentration unit is appropriate, press ENTER to

advance.

Press soft key to scroll through available

concentration unit choices. Press ENTER when

correct unit displays.

OPTIONS

menuok

Conc in mg/mL

Weight in kg

Dose in /kg/minmcg

OPTIONS

A B

menu ok

Dose in mcg/kg/min

Conc in mg/mL

Weight in kg

• If weight field appears and weight entry in kg

(kilograms) is desired, press ok soft key to advance to

programming page.

If weight entry in lb (pounds) is desired, press soft

then press ENTER. Press ok soft key to advance to

programming page. Patient weight in pounds is used

to automatically calculate dose per kilogram per time.

OPTIONS

A B

menu ok

Dose in mcg/kg/min

Conc in mg/mL

Weight in kg

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

58 Programming

AB OPTIONS

BolusOnly

Rate = - - - - - mL/h

Dose= - - - - - mg/kg/h

Conc= - - - - - mL/h

Wt= - - - - - kg

Primary Infusion - NO Guardrails® Suite MX Protection (Continued)

Dose Rate Calculation-Drug? NO DOSE LIMIT - Profiles

Feature Enabled (ON) (Continued)

Dose Rate Calculation-Profiles Feature Not Enabled (OFF)

This feature allows the clinician to select a drug name from

a pre-set list or to select a generic calculation feature by

selecting “Drug?” to calculate drug parameters for drugs

not on the list. If the preset list is disabled in the instrument

configuration settings, then only generic calculation is

available. Parameters are calculated automatically based on:

• concentration

• weight entry (if required)

• rate or dose entry

4. Enter parameters as needed.

• Dose field is highlighted for first entry but soft keys can

be used to highlight other parameters for entry prior to

dose. To automatically calculate dose instead of rate,

press rate soft key and enter a rate value. Once all

entries have been completed dose is automatically

calculated.

5. Verify that all parameters are correct and press ok soft

key to confirm.

• VTBI and VI setup page displays.

• VTBI field is highlighted.

6. To enter a VTBI value, use numeric data entry keys then

press ENTER key.

• VI field is highlighted.

7. If there is a VI value that needs to be cleared, press

CLEAR key or press 0 (zero) key then press ENTER key.

8. To continue programming, press ok soft key.

• RUN/HOLD page displays.

9. Verify that all parameters are correct and press run soft

key or RUN/HOLD key to start infusion.

10. To briefly view current setup parameters (concentration,

patient weight, current profile) from RUN/HOLD page or

during a running infusion, press 4 soft key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Primary Infusion - NO Guardrails® Suite MX Protection (Continued)

1. Press OPTIONS soft key.

• Options page appears.

2. Press Dose Rate Calculator soft key. OPTIONS

Resistance Trend

Monitoring Options

Set Pressure Baseline

return page

Dose Rate Calculator

OPTIONS

DOSE RATE MENU

Review/Resume

Enter New Program

Quit Program

3. Press Enter New Program soft key.

• An alphabetic pre-selection menu is displayed.

Dose Rate Calculation-Profiles Feature Not Enabled (OFF)

(Continued)

4. To use pre-selection menu press soft key corresponding

to first letter of desired drug.

5. Press soft key next to desired drug name to select it.

• page soft key(s) may be used to view additional

selections.

• If desired drug name is not listed, see “Drug? NO

DOSE LIMIT-Profiles Feature Enabled (On)”.

6. To approve all displayed information and advance to setup

page press ok soft key

To change concentration or weight units press soft key

next to parameter to be changed.

• soft key appears.

• To scroll through available selections, press soft

key. When desired unit displays, press ENTER key,

then press ok soft key to continue programming.

7. Pr e s s ok soft key to confirm selection and dosing units.

• Infusion setup page displays.

OPTIONS

A B

menu ok

Dose in mcg/kg/min

Conc in mg/mL

Weight in kg

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

60 Programming

Primary Infusion - NO Guardrails® Suite MX Protection (Continued)

Dose Rate Calculation-Drug? NO DOSE LIMIT - Profiles

Feature Not Enabled (OFF) (Continued)

8. To enter desired values, use numeric keys then press

ENTER key.

• Dose field is highlighted for first entry, but soft keys

can be used to highlight other parameters for entry

prior to dose. To automatically calculate dose

instead of rate, press Rate soft key and enter a rate

value. Once all entries have been competed, dose is

automatically calculated.

• Conc (concentration values of drug amount and

diluent volume) needs to be entered.

• If drug is weight-based, Wt (patient weight) needs to

be entered.

• If drug is not weight-based, Wt field does not appear.

9. When all fields have been completed, verify that all

parameters are correct and press ok soft key to confirm

• VTBI and VI setup page displays.

• VTBI field is highlighted.

10. To enter a VTBI value, use numeric data entry keys then

press ENTER key.

• VI field is highlighted.

11. If there is a VI value that needs to be cleared, press

CLEAR key or press 0 (zero) key then press ENTER key.

12. To continue programming, press ok soft key.

• RUN/HOLD page displays.

13. Verify that all parameters are correct and press run soft

key or RUN/HOLD key to start infusion.

14. To briefly view current dose rate setup parameters

(concentration, patient weight) from RUN/HOLD page or

during a running infusion, press 4 soft key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

OPTIONS

PRIMARY

Rate= 25.0 mL/h

VTBI= 10000 mL

VI= 1.0 mL

Loading Dose

This feature allows an initial infusion rate to be set up for a

specific volume, automatically followed by a maintenance

rate (primary settings) from the same container. If delivering

a bolus dose of medication to load prior to the start of a

continuous infusion, see "Primary Infusion - With Guardrails®

Suite MX Protection", "Bolus Dose". The primary VTBI and

VI include the loading dose volumes. When the loading dose

VTBI reaches zero, a transition tone sounds (if transition tone

feature is enabled), Load Dose Complete message displays

briefly, and the primary settings automatically take effect.

Verify the primary mode parameters prior to accessing the

Loading Dose option.

WARNING

This mode is useful for delivering

fluid challenges. This feature is for

delivery from primary containers

only. Using this feature with 2

separate containers may result in

unintended flow rates.

CAUTION

Guardrails® drug dosing limits

are available only within the

New Guardrails Drug or New

Guardrails IV Fluids option.

Dosing limits do not apply when

using Loading Dose programming.

Profile configurable options, as

defined in the Data Set, do apply.

Programming

1. Select desired channel, as necessary. Channel must be

on hold in primary mode.

2. Press OPTIONS key.

3. Press Loading Dose soft key.

• Loading Dose infusion rate is highlighted.

OPTIONS

Multi-Step

Multi-Dose

View Curr. Settings

return page

Loading Dose

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

62 Programming

Loading Dose (Continued)

Programming (Continued)

4. If current value is appropriate, press ENTER key.

To enter a new infusion rate, use numeric keypad and

press ENTER key.

• Loading Dose VTBI is highlighted.

NOTE:

À The Loading Dose VTBI must be less than the primary VTBI.

OPTIONS

LOADING DOSE

Primary Settings

Rate= mL/h200.0

VTBI= mL500.0

OPTIONS

LOADING DOSE

Rate= mL/h200.0

VTBI= 500.0 mL

Primary Settings

10% Resistance

OPTIONS

LOADING DOSE

VTBI= mL500.0

Primary Settings

Rate= mL/h200.0

5. If current value is appropriate, press ENTER key.

To enter a new VTBI, use numeric keypad and press

ENTER key. À

6. To start loading dose infusion, press RUN/HOLD key.

7. To briefly view current profile press 4 soft key.

8. To briefly view primary settings (Pri Rate, Pri VTBI, Total

VI) during loading dose infusion, press Primary Settings

soft key.

9. To change Primary Settings during a loading dose

infusion, press Primary Settings soft key.

10. Press soft key next to parameter to be edited.

• Current value is highlighted.

11. Make changes:

a. To enter a new value, use numeric keypad.

b. To reset volume infused to 0.0 mL, press CLEAR or 0

(zero) key.

12. To accept new value, press ENTER key.

13. When complete:

• Loading Dose Complete is displayed.

• Pump returns to Primary Infusion.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Multi-Dose

This feature allows 1 to 24 infusions to be preprogrammed with

the same rate and volume, to be delivered at equally spaced

intervals, over a period of up to 24 hours. It also offers a

delayed start option up to 8 hours and a Dose Complete Alert

Option. These features can be turned on or off.

This program requires another infusing line to keep the vein

open between programmed doses since there is no KVO

infusion between doses or following program completion.

CAUTION

Guardrails® drug dosing limits

are available only within the

New Guardrails Drug or New

Guardrails IV Fluids option.

Dosing limits do not apply when

using Multi-Dose programming.

Profile configurable options, as

defined in the Data Set, do apply.

Programming

1. Select desired channel, as necessary. Channel must be

on hold in primary mode.

2. Press OPTIONS key.

3. Press Multi-Dose soft key.

OPTIONS

Rate= 25.0 mL/h

VTBI= 4.0 mL

VI= 0.0 mL

Primary

OPTIONS

Multi-Step

Multi-Dose

View Curr. Settings

return page

Loading Dose

4. Press Enter New Program soft key. OPTIONS

A B

MULTI-DOSE MENU

Review/Resume

Enter New Program

Quit Program

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

64 Programming

Multi-Dose (Continued)

Programming (Continued)

• Setup page appears with infusion rate highlighted.

OPTIONS

A B

Rate=250.0 mL/h

VTBI/Dose= ----- mL

No. Doses= --

Frequency= -- h

OPTIONS

A B

Rate=250.0 mL/h

VTBI/Dose=100.0 mL

No. Doses= --

Frequency= -- h

OPTIONS

A B

Rate=250.0 mL/h

VTBI/Dose=100.0 mL

No. Doses= 4

Frequency= -- h

OPTIONS

A B

Rate= ----- mL/h

VTBI/Dose= ----- mL

No. Doses= --

Frequency= -- h

6. To enter VTBI/Dose, use numeric keypad. Press ENTER

key.

7. To enter number of doses, use numeric keypad. Press

ENTER key.

5. To enter infusion rate, use numeric keypad. Press ENTER

key.

8. To enter dose frequency (time interval from start of one

dose until start of next), use numeric keypad. Press

ENTER key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Multi-Dose (Continued)

Programming (Continued)

9. Verify that all parameters are correct then press ok soft

key.

• If Dose Complete Alert Option is enabled, DOSE

COMPLETE ALERT OPTION page appears.

10. To select On or Off, use soft keys.

11. To continue programming, press ok soft key. À

• To start first dose immediately, see “Starting First

Dose Immediately After Programming”.

• To delay start of first dose, see “Delaying Start of First

Dose”.

NOTE:

À All doses must be programmed to start within 24 hours.

OPTIONS

A B

Rate=250.0 mL/h

VTBI/Dose=100.0 mL

No. Doses= 4

Frequency= 6 h

OPTIONS

A B

DOSE COMPLETE

ALERT OPTION

Off

OPTIONS

A B

DOSE COMPLETE

ALERT OPTION

Off

Starting First Dose Immediately After

Programming

1. A displayed time of 0 hours, 0 minutes identifies that first

dose starts immediately after programming.

2. To approve and advance to main hold page, press ok soft

key.

OPTIONS

A B

0 h

0 min

Until First Dose

VI= 0.0 mL

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

66 Programming

Multi-Dose (Continued)

Programming (Continued)

Starting First Dose Immediately After

Programming (Continued)

3. To start infusion, press RUN/HOLD key or run soft key.

Delaying Start of First Dose

1. To enter number of hours until first dose, use numeric

keypad. Press ENTER key.

OPTIONS

A B

run

Rate=250.0 mL/h

VTBI=100.0 mL

VI= 0.0 mL

Dose 1 of 4

2. To enter number of minutes (0 to 59) until first dose, use

numeric keypad. Press ENTER key.

3. To advance to timer hold page, press start timer soft key.

OPTIONS

A B

0 h

0 min

Until First Dose

VI= 0.0 mL

OPTIONS

A B

start timer

3 h

12 min

Until First Dose

VI= 0.0 mL

OPTIONS

A B

start timer

3 h

0 min

Until First Dose

VI= 0.0 mL

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

OPTIONS

stop timer

12 min

Until First Dose

Multi-Dose (Continued)

OPTIONS

Rate=250.0 mL/h

VTBI=100.0 mL

100.0mL @250.0mL/h

h x 4 VI=100.0

Adult ICU

Changing Time Interval Until Next Dose

1. Press stop timer soft key.

2. To select a value for editing, press a soft key.

OPTIONS

stop timer

12 min

Until Dose 2 of 4

OPTIONS

A B

start timer

3 h

12 min

Until Dose 2 of 4

VI= 100.0 mL

Programming (Continued)

Delaying Start of First Dose (Continued)

• Hourglass icon flashes to indicate timer is counting

down to start of dose.

• Dose automatically starts its infusion when timer

reaches 0 hours, 0 minutes.

4. To briefly view Multi-Dose programmed information, press

4 soft key.

OPTIONS

A B

start timer

2 h

12 min

Until Dose 2 of 4

VI= 100.0 mL

3. To enter new value, use numeric keypad. Press ENTER

key.

4. When editing is complete, press start timer soft key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

68 Programming

OPTIONS

A B

Return To

Multi-Dose?

no yes

Multi-Dose (Continued)

Resuming an Interrupted Multi-Dose

1. Select desired channel, as necessary.

2. Select New Patient and Profile Options, as necessary. À

• Return To Multi-Dose? page appears.

3. Press yes soft key.

OPTIONS

A B

MULTI-DOSE MENU

Review/Resume

Enter New Program

Quit Program

If Infusion Was in Progress When

Interrupted

1. To approve and advance to main hold page, press ok soft

key.

OPTIONS

A B

Rate=250.0 mL/h

VTBI/Dose=100.0 mL

Frequency= 6 h

DOSE 1 INCOMPLETE

OPTIONS

A B

run

Rate=250.0 mL/h

VTBI=80.0 mL

VI= 20.0 mL

DOSE 1 of 4

2. To resume infusion, press RUN/HOLD key or run soft key.

• Pressing no soft key returns screen to primary setup

page.

4. To access setup parameters, press Review/Resume soft

key.

• If infusion was in progress when interrupted, see "If

Infusion Was In Progress When Interrupted”.

• If infusion was not in progress when interrupted, see “If

Infusion Was Not In Progress When Interrupted”.

NOTE:

À Previous programming parameters will be preserved only

if current profile is accepted and NEW PATIENT?-NO is

selected.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Multi-Dose (Continued)

Resuming an Interrupted Multi-Dose (Continued)

If Infusion Was Not in Progress When

Interrupted

1. Press ok soft key. OPTIONS

A B

Rate=250.0 mL/h

VTBI/Dose=100.0 mL

Frequency= 6 h

DOSE 1 COMPLETE

OPTIONS

A B

start timer

2 h

4 min

Until Dose 2 of 4

VI= 100.0 mL

2. Edit time to delivery of next dose, as necessary.

3. To begin timer’s countdown to delivery of next dose, press

start timer soft key.

Multi-Step

The Multi-Step feature allows a sequential drug delivery

program (up to 9 steps) to be set, delivering volumes of fluid

at different rates during each step. This allows the instrument

parameters to be set up once and to deliver a sequence

eliminating the need to change the rate and VTBI after each

infusion step.

The infusion may be programmed in either rate and volume or

volume and time. At completion of the last programmed step,

the channel switches to the preset KVO rate or remains at the

current rate, whichever is less.

CAUTION

Guardrails® drug dosing limits

are available only within the

New Guardrails Drug or New

Guardrails IV Fluid option. Dosing

limits do not apply when using

Multi-Step programming. Profile

configurable options, as defined in

the Data Set, do apply.

Programming

1. Select desired channel, as necessary. Channel must be

on hold in primary mode.

2. Press OPTIONS key.

4. When final dose is complete:

• Dose _ of _ Complete displays until user takes

action.

• No Continuous Infusion or KVO Rate occurs.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

70 Programming

Multi-Step (Continued)

3. Press Multi-Step soft key.

OPTIONS

A B

PROGRAMMING OPTIONS

Rate and Volume

Volume and Time

4. Press Enter New Program soft key.

OPTIONS

Multi-Step

Multi-Dose

View Curr. Settings

return page

LoadingDose

OPTIONS

A B

MULTI-STEP MENU

Review/Resume

Enter New Program

Quit Program

Programming by Rate and Volume

1. Press Rate and Volume soft key.

• Step 1 of infusion sequence displays.

OPTIONS

A B

PROGRAMMING OPTIONS

Rate and Volume

Volume and Time

OPTIONS

A B

STEP 1

Rate= -------- mL/h

VTBI= ----- mL

Time= -- h -- min

Programming (Continued)

5. Determine setup method:

• Rate and Volume: Instrument calculates step

infusion time. Proceed to "Programming by Rate and

Volume".

• Volume and Time: Instrument calculates rate.

"Proceed to Programming by Volume and Time".

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Multi-Step (Continued)

Programming (Continued)

3. To enter VTBI, use numeric keypad. Press ENTER key.

• Time in hours and minutes is automatically calculated

and displayed.

4. To approve all displayed information and advance to step

2 of infusion sequence, press ok soft key.

2. To enter a rate, use numeric keypad. Press ENTER key.

5. To set up each additional step of infusion sequence,

repeat steps 2 through 4.

6. When all steps have been entered and accepted, press

done soft key.

• Review page(s) display 3 sequence steps at a time.

OPTIONS

A B

STEP 1

Rate= 25.0 mL/h

VTBI= ----- mL

Time= -- h -- min

OPTIONS

A B

STEP 1

Rate= 25.0 mL/h

VTBI= 5.0 mL

Time= 0 h 12 min

OPTIONS

A B

STEP 4

Rate= ----- mL/h

VTBI= ----- mL

Time= -- h -- min

done

Programming by Rate and Volume

(Continued)

OPTIONS

# RATE VTBI TIME

1 25.0 5.0 0h12m

2 50.0 25.0 0h30m

3 100.0 100.0 1h 0m

okmenu

7. To approve and advance through review page(s), press ok

soft key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

72 Programming

Multi-Step (Continued)

Programming (Continued)

Programming by Rate and Volume

(Continued)

OPTIONS

A B

STEP TOTALS (3)

VTBI= 130.0 mL

Time= 1 h 42 min

VI 25.0 mL

8. To clear VI, if desired, press CLEAR or 0 (zero) key.

Press ENTER key.

OPTIONS

A B

STEP TOTALS (3)

VTBI= 130.0 mL

Time= 1 h 42 min

VI 0.0 mL

9. To accept STEP TOTALS page, press ok soft key.

10. To start Multi-Step infusion program, press run soft key or

RUN/HOLD key.

OPTIONS

A B

runsetup

STEP 1 of 3

Rate= 25.0 mL/h

VTBI= 5.0 mL

VI= 0.0 mL

Programming by Volume and Time

1. Press Volume and Time soft key OPTIONS

A B

PROGRAMMING OPTIONS

Rate and Volume

Volume and Time

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Multi-Step (Continued)

Programming (Continued)

OPTIONS

A B

STEP 1

Rate= ----- mL/h

VTBI= ----- mL

Time= -- h -- min

• Step 1 of infusion profile displays.

• VTBI is highlighted.

2. To enter VTBI, use numeric keypad. Press ENTER key.

• Time (hours) is highlighted.

3. To enter hours, use numeric keypad. Press ENTER key.

• Time (minutes) is highlighted.

OPTIONS

A B

STEP 1

Rate= ----- mL/h

VTBI= 5.0 mL

Time= -- h -- min

OPTIONS

STEP 1

Rate= ----- mL/h

VTBI= 5.0 mL

Time= 0 h -- min

Programming by Volume and Time

4. To enter minutes (0-59), if desired, use numeric keypad.

Press ENTER key.

• Volumetric rate is automatically calculated and

displayed.

5. To approve all displayed information and advance to STEP

2 of infusion profile, press ok soft key.

OPTIONS

A B

STEP 1

Rate= 25.0 mL/h

VTBI= 5.0 mL

Time= 0 h 12 min

6. To set up each additional step of infusion profile, repeat

steps 1 through 4.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

74 Programming

Multi-Step (Continued)

Programming (Continued)

7. When all steps have been entered and accepted, press

done soft key.

• Review page(s) display 3 profile steps at a time.

8. To approve and advance through review page(s), press ok

soft key.

OPTIONS

A B

STEP 4

Rate= ----- mL/h

VTBI= ----- mL

Time= -- h -- min

done

Programming by Volume and Time

(Continued)

OPTIONS

# RATE VTBI TIME

1 25.0 5.0 0h12m

2 50.0 25.0 0h30m

3 100.0 100.0 1h 0m

okmenu

9. To clear VI, if desired, press CLEAR or 0 (zero) key.

Press ENTER key.

10. To approve STEP TOTALS page, press ok soft key.

OPTIONS

A B

STEP TOTALS (3)

VTBI= 130.0 mL

Time= 1 h 42 min

VI 25.0 mL

OPTIONS

A B

STEP TOTALS (3)

VTBI= 130.0 mL

Time= 1 h 42 min

VI 0.0 mL

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Multi-Step (Continued)

Programming (Continued)

Programming by Volume and Time

(Continued)

11. To start Multi-Step infusion program, press RUN/HOLD

key or run soft key.

OPTIONS

A B

run

setup

STEP 1 of 3

Rate= 25.0 mL/h

VTBI= 5.0 mL

VI= 0.0 mL

Making Changes During Multi-Step

Select the desired channel, as necessary. The channel does

not need to be on hold to clear the VI or to view the totals

remaining.

Clearing Volume Infused

1. Press VI soft key. OPTIONS

A B

STEP 1 of 3

10% Resistance

Rate= 25.0 mL/h

VTBI= 4.0 mL

VI= 1.0 mL

2. Press CLEAR or 0 (zero) key.

3. Press ENTER key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

76 Programming

Multi-Step (Continued)

Viewing Totals Remaining

Press 4 soft key. OPTIONS

A B

STEP 2 of 3

10% Resistance

Rate= 50.0 mL/h

VTBI= 25.0 mL

VI= 5.0 mL

OPTIONS

Rate= 50.0 mL/h

VTBI= 25.0 mL

Totals Remaining

VTBI= 125.0 mL

Time= 1 h 30 min

Adult ICU

• Time and VTBI remaining in Multi-Step program display for

a short interval.

Viewing or Editing

The channel must be on hold to view or edit the steps in the

program.

1. To place channel on hold, press RUN/HOLD key.

2. To return to review page(s), press setup soft key.

• A tick mark (y) next to a step on review page(s)

indicates it has not started.

• Only steps having a (y) can be edited.

• Completed steps, or a step in progress, do not have

a (y).

• A step number in progress is highlighted.

3. To advance through review page(s) of program, press ok

soft key.

OPTIONS

A B

runsetup

STEP 1 of 3

Rate= 25.0 mL/h

VTBI= 4.0 mL

VI= 1.0 mL

# RATE VTBI TIME

1 25.0 5.0 0h12m

2 50.0 25.0 0h30m

3 100.0 100.0 1h 0m

OPTIONS

A B

Making Changes During Multi-Step (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Multi-Step (Continued)

Making Changes During Multi-Step (Continued)

4. To select a step for editing, press a soft key.

5. To select value for editing, press a soft key.

6. To enter new value, use numeric keypad. Press ENTER

key.

7. To return to review page(s) when programming is

complete, press ok soft key.

Viewing or Editing (Continued)

8. To approve review page(s) and STEP TOTALS page,

press ok soft key.

OPTIONS

A B

STEP 2

Rate= 50.0 mL/h

VTBI= 25.0 mL

Time= 0 h 30 min

9. To resume infusion, press RUN/HOLD key or run soft key.

OPTIONS

A B

STEP 2

Rate= 25.0 mL/h

VTBI= 25.0 mL

Time= 1 h 00 min

# RATE VTBI TIME

1 25.0 5.0 0h12m

2 25.0 25.0 1h00m

3 100.0 100.0 1h 0m

OPTIONS

A B

OPTIONS

A B

run

setup

STEP 1 of 3

Rate= 25.0 mL/h

VTBI= 4.0 mL

VI= 1.0 mL

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

78 Programming

Multi-Step (Continued)

3. Press yes soft key.

• Pressing no soft key returns screen to primary setup

page.

4. Press Review/Resume soft key.

Resuming an Interrupted Multi-Step

The channel retains its place in the program if the instrument

is turned off. The program can be restarted from step 1 or

resumed where it left off.

1. Select desired channel, as necessary.

2. Select New Patient and Profile Options, as necessary. À

• Return To Multi-Step? page appears.Á

OPTIONS

A B

Return To

Multi-Step?

no yes

OPTIONS

A B

MULTI-STEP MENU

Review/Resume

Enter New Program

Quit Program

5. To resume program from point of interruption, press

Continue Program soft key.

To restart program at beginning of step 1, press Restart

Program soft key.

6 Verify all settings are correct. If a change is required, see

“Making Changes During Multi-Step”.

OPTIONS

A B

STEP 1 of 3

In Progess

Continue Program

Restart Program

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Multi-Step (Continued)

7. To approve review page(s) and STEP TOTALS page,

press ok soft key.

Resuming an Interrupted Multi-Step (Continued)

NOTES:

À Previous programming parameters will be preserved only

if current profile is accepted and NEW PATIENT?-NO is

selected.

Á If resuming an infusion on a dual channel instrument with an

infusion currently running, display goes directly to Return To

Multi-Step? during startup.

OPTIONS

A B

run

setup

STEP 1 of 3

Rate= 25.0 mL/h

VTBI= 4.0 mL

VI= 1.0 mL

# RATE VTBI TIME

1 25.0 5.0 0h12m

2 25.0 25.0 1h00m

3 100.0 100.0 1h 0m

OPTIONS

A B

Quitting Multi-Dose and Multi-Step

The channel must be on hold or the last dose complete.

1. Press menu soft key. OPTIONS

A B

run

setup

STEP 1 of 3

Rate= 25.0 mL/h

VTBI= 4.0 mL

VI= 1.0 mL

NOTE:

À Primary setup page parameters may be different from those of

the Multi-Dose or Multi-Step program. Verify all settings prior

to resuming an infusion.

2. To return to primary setup page, press Quit Program soft

key. À

OPTIONS

A B

MULTI-STEP MENU

Review/Resume

Enter New Program

Quit Program

8. To continue or restart program, press RUN/HOLD key or

run soft key.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

80 Programming

Secondary Infusion - NO Guardrails® Suite MX Protection

Introduction

Basic Secondary Infusion- Profiles Feature Enabled (On)

Primary infusion must be on hold to program secondary

infusion.

Secondary mode must be set to ON in the instrument system

configuration settings. If secondary mode is OFF an invalid

keypress tone sounds and "Secondary Not Allowed" displays

when the SEC key is pressed.

1. Press SEC key

• Secondary Menu displays

2. Press Basic SEC soft key

• Basic secondary programming page displays.

• VTBI field is highlighted.

3. To enter desired VTBI, use numeric keys then press

ENTER key.

• VI field is highlighted.

4. If there is a VI value that needs to be cleared, press

CLEAR key or press 0 (zero) key then press ENTER key.

• Time is highlighted.

5. To enter a value, use numeric data entry keys to enter

hours (0-99), then minutes (0-59). Press the ENTER key

to accept each entry.

• Time can be entered to calculate rate or if rate entry

is desired, press rate - time soft key. It changes to

rate - time, indicating that rate may be entered.

6. To continue programming press ok soft key.

• A Secondary Clamp reminder message displays.

See “Secondary Infusion With Guardrails® Suite MX

Protection, Introduction and Setup".

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Programming

Secondary Infusion - NO Guardrails® Suite MX Protection (Continued)

Basic Secondary Infusion- Profiles Feature Enabled (On)

(Continued)

AB OPTIONS

IS SECONDARY CLAMP

OPEN?

yes

Basic Secondary Infusion- Profiles Feature

Not Enabled (Off)

1. Press SEC key

• Secondary setup page displays.

• Secondary rate is highlighted.

2. If current secondary infusion rate is appropriate, press

ENTER key.

To enter a new rate, use numeric keypad then press

ENTER key.

• Maximum rate for secondary infusion is 600 mL/h.

• Secondary VTBI is highlighted.

3. If Secondary VTBI is appropriate, press ENTER key.

To enter a new VTBI, use numeric keypad then press

ENTER key.

7. Verify that secondary clamp is open before proceeding,

then press yes soft key.

• Basic secondary RUN/HOLD page displays.

8. Verify that all parameters are correct and press run soft

key or RUN/HOLD key to start infusion.

9. To briefly view primary parameters (Pri rate, Pri VTBI) and

current profile from RUN/HOLD page or during a running

infusion, press 4 soft key.

10. When secondary infusion is complete:

• An audio tone sounds (if enabled).

• Channel _ Secondary Complete briefly displays.

• Infusion automatically transitions to primary rate.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

82 Programming

Secondary Infusion - NO Guardrails® Suite MX Protection (Continued)

Basic Secondary Infusion- Profiles Feature

Not Enabled (Off) (Continued)

4. To start secondary infusion, press RUN/HOLD key.

• Secondary clamp reminder message displays.

5. Verify that secondary clamp is open before proceeding,

then press yes soft key.

6. To briefly view primary settings during secondary infusion

press Primary Settings soft key.

• Primary rate (PriRate), primary volume to be infused

(PriVTBI) and total volume infused (ToalVI) are

displayed.

• Display returns to normal secondary page after 6

seconds.

7. To change Primary settings, press soft key for Pri Rate,

Pri VTBI or Total VI to freeze display and highlight

desired value, then edit as usual (see "Primary Infusion

- With Guardrails® Suite MX Protection", "Making Changes

During Continuous Infusion").

8. When secondary infusion is complete:

• An audio tone sounds (if enabled).

• Channel _ Secondary Complete briefly displays.

• Infusion automatically transitions to primary rate.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

Monitoring Options - General

All features and options in this section are shown enabled.

Options are enabled through the hospital Data Set profile

configuration settings, or through the instrument configuration

settings if the Profiles feature is not enabled (OFF).

The Dynamic Monitoring System provides the ability to monitor

downstream pressure or resistance, allowing rapid detection of

full and partial occlusions. Resistance monitoring eliminates

the impact of patient elevation and flow rate to provide the

most direct assessment of patency. Components of this

system are:

• Monitoring Options: to select IV line/site monitoring

modes of resistance, high resistance, and adjustable or

fixed pressure.

• Auto Restart Plus Feature: allows instrument to

automatically resume operation when specific instrument

operating conditions are met.

• Adjustable Resistance Alert: to provide an early

warning of increases in downstream flow resistance.

• Adjustable Pressure Alarm: to provide an early warning

of increases in downstream pressure.

• Trend Graph: to display downstream pressure or flow

resistance over time.

• Pressure Baseline: to provide a starting point from which

to measure changes in system pressure.

IV lines, catheters, and applications create various levels of

resistance to flow. Monitoring mode options are available to

meet each clinical need.

• Resistance: designed to monitor IV line/site resistance

providing optimum sensitivity for most IV applications.

• High Resistance: designed to monitor IV line/site

resistance with optimum sensitivity where higher resistance

catheters are used.

OPTIONS

Rate= 125.0 mL/h

VTBI=1000.0 mL

VI= 0.0 mL

Primary

50% Resistance

Resistance Monitoring

WARNINGS

• The SE Pump is designed to

stop fluid flow under alarm

conditions. Periodic patient

monitoring must be performed to

ensure the infusion is proceeding

as expected. It is a positive

displacement delivery system,

capable of developing positive

fluid pressures to overcome

widely varying resistances to

flow encountered in practice,

including resistances to flow

imposed by small gauge

catheters, filters and intra-arterial

infusion. It is neither designed

nor intended to detect infiltrations

and will not alarm under

infiltration conditions.

• Before each use, verify the

pressure or resistance alarm

limits are appropriate for the

patient.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

84 Dynamic Monitoring System

Monitoring Options - General (Continued)

• Adjustable Pressure: designed to monitor IV line/

site pressure and provide user-adjustable pressure

alarm limits. Used for Precision Flow mode or for high

resistance systems; such as, infusion through transducers,

into dialysis systems and through highest resistance

catheters. À

• Pressure: designed to monitor IV line/site pressure and

alarm based on a fixed pressure limit. À

NOTE:

À Precision Flow: in fixed and adjustable pressure modes, the

SE Pump provides enhanced flow continuity at rates below

50 mL/h.

Selecting Monitoring Option

For dual channel instruments, select the desired channel

as necessary. The bar graph and numeric displays are not

available when the split screen is displayed.

1. Press OPTIONS key.

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

450 mmHg

Pressure Monitoring

OPTIONS

Rate= 125.0 mL/h

VTBI=1000.0 mL

VI= 0.0 mL

Primary

Limit=250 mmHg

2. Press Monitoring Options soft key. OPTIONS

Resistance Trend

Monitoring Options

Set Pressure Baseline

return page

Guardrails Library

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

WARNING

Each time the instrument is

turned on, verify and/or set the

monitoring mode, resistance alert

and/or pressure alarm limit. If the

monitoring mode, resistance alert

and/or pressure alarm limit are not

verified, the instrument may not be

operating with the desired occlusion

detection parameter(s).

Monitoring Options - General (Continued)

Selecting Monitoring Option (Continued)

3. Press soft key for Resistance, High Resistance or

Adjustable Pressure. À

OPTIONS

A B

Monitoring Options

Resistance

High Resistance

Adjustable Pressure

4. Press ok soft key. Display automatically returns to normal

operating screen. Á

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

50% Resistance

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

50% Hi Resist.

a. If Resistance option is selected, % Resistance

displays below bar graph while infusing. Â

b. If High Resistance option is selected, % Hi Resist.

displays below bar graph while infusing. Ã

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

86 Dynamic Monitoring System

NOTES:

À If pressure limit adjustment is available, selection reads

Adjustable Pressure; otherwise, it reads Pressure.

Á While the channel is on, the selected option, resistance alert

and pressure alarm thresholds remain in effect until changed

by the operator.

Â Resistance alert limit may be adjusted using the soft keys

located below the arrow symbols (see "Monitoring Options

- Resistance Mode", “Resistance Alert”).

Ã High Resistance alert limit may be adjusted using the soft

keys located below the arrow symbols.

Ä Pressure alarm limits may be adjusted when operating in

Adjustable Pressure mode using the soft keys located below

the arrow symbols (see "Monitoring Options - Pressure Mode",

“Adjustable Pressure Alarm”).

Å Maximum pressure limit settings may be configured by

qualified service personnel.

Monitoring Options - General (Continued)

Selecting Monitoring Option (Continued)

Detection of Downstream Occlusions

In the Resistance or High Resistance monitoring mode, a

RESISTANCE ALERT condition occurs when the measured

resistance reaches the alert limit.

Monitoring Options - Resistance Mode

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

Limit=250 mmHg

c. If Adjustable Pressure option is selected, pressure

system accuracy can be enhanced by ensuring no

occlusion or other pressure source exists in IV line

when activating RUN/HOLD. Ä Å

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Resistance Alert

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

Detection of Downstream Occlusions (Continued)

Monitoring Options - Resistance Mode (Continued)

An OCCLUSION DOWNSTREAM condition is detected when

the measured resistance reaches 100% of scale. For the

Resistance mode, 100% results from a resistance producing

2 mmHg per mL/h of flow. For the High Resistance mode,

100% results from a resistance producing 6 mmHg per mL/h

flow.

An OCCLUSION DOWNSTREAM condition is also detected

when the configured pressure limit is exceeded. This limit

may be set, by qualified service personnel, from 1 mmHg to

600 mmHg ( Pressure Limit, Maximum).

When a Downstream Occlusion is detected, one of the

following responses occur:

• If Auto Restart Plus feature is on, Checking Line message

displays and audible tone sounds.

• If Auto Restart Plus feature is off, OCCLUSION

DOWNSTREAM alarm occurs.

OPTIONS

A B

run

OCCLUSION

DOWNSTREAM

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Checking Line

Auto Restart Plus Feature

The Auto Restart Plus feature provides the ability to

automatically continue an infusion if downstream resistance or

pressure measurements indicate that an occlusion condition

has cleared within a 40-second Checking Line period

(excluding High Resistance Monitoring mode).

The Checking Line message and tone are presented when

a resistance measurement exceeds the alarm threshold of

100%.

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Checking Line

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

88 Dynamic Monitoring System

Monitoring Options - Resistance Mode (Continued)

Resistance Alert

The Resistance Alert provides an early warning of increasing

flow resistance. The Resistance Alert marker can be set from

0% to 100% of scale in 5% increments. This feature can be

enabled or disabled and a power-on default alert level is set

through the hospital Data Set.

To optimize the alert feature, it is advisable to set the alert level

20-30% higher than the initial displayed resistance. Read the

resistance approximately 2 minutes after starting an infusion.

Setting Alert Marker

To numerically display present alert level marker, press either

or soft key. Vertical line on resistance bar graph visually

indicates alert level.

Each additional press of either arrow soft key increases or

decreases alert level marker and numeric value by 5%.

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

90% Resistance

OPTIONS

A B

run

OCCLUSION

DOWNSTREAM

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

Alert = 70%

If resistance measurements initiate the Checking Line

condition, the channel continues infusing in order to

determine if the measured flow resistance has changed. If

the measured flow resistance falls to any value below 100%

within 40 seconds, the channel automatically resumes normal

operating conditions (excluding High Resistance Monitoring

mode).

Pressure measurements initiate the Checking Line period

when the pressure exceeds the configured limit. If the

pressure falls to less than one-third of the configured limit

within 40 seconds, normal flow resumes. If the condition is not

cleared, the OCCLUSION DOWNSTREAM alarm occurs and

infusion stops until manually restarted.

This feature can be configured through the hospital Data

Set to allow from 1 to 9 Checking Line restarts. After the

programmed number of restarts has occurred or the 40-

second Checking Line period has been exceeded, the

channel immediately alarms OCCLUSION DOWNSTREAM

when resistance or pressure conditions indicate an occlusion.

Auto Restart Plus Feature (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

Monitoring Options - Resistance Mode (Continued)

If Flow Resistance Exceeds Alert Level

Marker

If flow resistance exceeds the alert level marker, a Resistance

Alert message displays and an alert tone sounds. The

channel continues to infuse, and the message and tone

continue until one of the following resistance levels occurs:

• IV line/site resistance falls below alert level marker.

• Resistance alert level marker increases above current

measured resistance value.

• Resistance rises to 100%, initiating a Checking Line or

OCCLUSION DOWNSTREAM condition.

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Resistance Alert

Resistance Trend Graphs

In Resistance and High Resistance monitoring modes, a trend

graph displays flow resistance over time. Trend graphs of

15 minutes, 1 hour, 4 hours and 12 hours are available during

normal operation when enabled through the hospital Data Set.

Downstream Occlusions are indicated by a tick mark (y) at the

top of the trend screen.

Viewing Graphs

For dual channel instruments, select the desired channel, as

necessary. The trend graph is not available while the split

screen is displayed.

1. Press OPTIONS key.

OPTIONS

A B

return time

clear

RESISTANCE

now

-12h

100%

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

25% Resistance

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

90 Dynamic Monitoring System

Monitoring Options - Resistance Mode (Continued)

2. Press Resistance Trend soft key. OPTIONS

Resistance Trend

Monitoring Options

Set Pressure Baseline

return page

Guardrails Library

3. To change graph time frame, press time soft key.

• A dashed horizontal line represents current resistance

alert level.

• Gaps in graph may indicate noninfusing conditions;

such as, turned off, on hold, in alarm.

• If channel has been placed in Pressure Monitoring

mode for some portion of a trend graph window,

resistance data is not available and zero values are

plotted.

• A tick mark (y) at top of graph indicates an occlusion.

• When viewing Resistance Trend Graphs in High

Resistance mode, HI RESIST displays under graph.

OPTIONS

return time

clear

HI RESIST now-12h

100

Clearing Graphs

1. To clear graphed data, press clear soft key. OPTIONS

return time

clear

RESISTANCE now-12h

100

OPTIONS

A B

return time

clear

RESISTANCE

now

-12h

100%

Viewing Graphs (Continued)

Resistance Trend Graphs (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

Monitoring Options - Resistance Mode (Continued)

Resistance Trend Graphs (Continued)

Clearing Graphs (Continued)

2. Press ok soft key.

• All data is cleared from graphs.

Returning to Normal Operating Screen

Press return soft key.

• Normal operating screen appears.

Following events also turn off trend graph:

• Pressing RUN/HOLD key.

• An alarm.

• Dual channel instrument: pressing A B .

• Dual channel instrument: replaced with a split screen

display after 1 minute if both channels are infusing.

OPTIONS

return time

clear

RESISTANCE now-12h

100

AB OPTIONS

All trend data

will be cleared

return

OPTIONS

return time

clear

RESISTANCE now-12 h

100

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

33% Resistance

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

92 Dynamic Monitoring System

Monitoring Options - Pressure Mode

Detection of Downstream Occlusions

When using the Adjustable Pressure monitoring mode, a

pressure alarm limit may be selected, in 25 mmHg increments,

from 25 mmHg to the maximum configured pressure limit.

When measured pressure exceeds this level, an OCCLUSION

DOWNSTREAM condition occurs.

When a Downstream Occlusion is detected, one of following

responses occurs:

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

500 mmHg

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Checking Line

OPTIONS

A B

run

OCCLUSION

DOWNSTREAM

600 mmHg

• If Auto Restart Plus feature is on, a Checking Line

message appears, along with an audible tone. (Reference

“Auto Restart Plus Feature” for further details.)

The Auto Restart Plus feature provides the ability to

automatically continue an infusion if downstream pressure

measurements indicate that an occlusion condition has cleared

within a 40-second Checking Line period (excluding High

Resistance Monitoring mode).

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Checking Line

• If Auto Restart Plus feature is off, an OCCLUSION

DOWNSTREAM alarm occurs.

Auto Restart Plus Feature

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

Monitoring Options - Pressure Mode (Continued)

Auto Restart Plus Feature (Continued)

OPTIONS

A B

run

OCCLUSION

DOWNSTREAM

The Checking Line message and tone occur whenever a

pressure measurement exceeds the selected alarm threshold.

If the pressure falls to less than one-third of the alarm limit

within 40 seconds, normal flow resumes. The Adjustable

Pressure mode allows control of the pressure alarm limit. If

the condition is not cleared, the OCCLUSION DOWNSTREAM

alarm occurs and infusion stops until manually restarted.

This feature can be configured through the hospital Data

Set to allow from 1 to 9 Checking Line restarts. After the

programmed number of restarts has occurred or the 40-

second Checking Line period has been exceeded, the

channel immediately alarms OCCLUSION DOWNSTREAM

when resistance or pressure conditions indicate an occlusion.

Adjustable Pressure Alarm

In the Adjustable Pressure monitoring mode, the pressure

alarm limit may be varied from 25 mmHg to the maximum

configured pressure limit, in 25 mmHg increments. A default

alarm level and a maximum pressure limit are set through the

hospital Data Set profile configuration settings or through the

instrument confirmation settings if the Profiles feature is not

enabled (OFF).

Setting Alarm Limit Marker

Pressing either arrow ( or ) soft key changes alarm limit by

25 mmHg in corresponding direction. It is advisable to select

an alarm limit appropriate for flow rate. At lower flow rates,

alarm limit should be set lower, to shorten time to alarm.

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

Limit = 450mmHg

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

94 Dynamic Monitoring System

Monitoring Options - Pressure Mode (Continued)

Pressure Monitoring Using Automatic

Baseline Calibration

The auto pressure baseline calibration remains in effect until

the instrument is turned off, the latch is opened, the set is

reloaded, or the Set Pressure Baseline function is performed.

• First activation of RUN/HOLD for a new infusion

automatically establishes a pressure baseline based

on current system pressure. An optimal baseline is

maintained upon subsequent activations of RUN/HOLD, as

follows:

- If current system pressure is same or higher than

original baseline, pressure baseline does not change.

- If current system pressure is less than original baseline,

system automatically resets to new system pressure

value.

• Pressure measurement can be optimized, particularly

at low flow rates (less than 3 mL/h), by pausing and

restarting at least once every 2 hours (for example, when

reprogramming VTBI). This allows pressure baseline to

calibrate based on current system pressure.

• Prior to activation, ensure that pressure has not built

up in IV line due to either occlusion or flow from other

instruments through a common catheter. This will result in

a more accurate pressure measurement.

• When loading a set connected to a small diameter catheter,

wait at least 5 seconds after loading set before activating

RUN/HOLD. This allows pressure generated by loading

process to dissipate and sensor to stabilize. (Very small

PICC catheters; such as, 28 gauge/1.2 French, may require

60 seconds or more for stabilization.)

• When multiple instruments are infusing through a common

small diameter catheter, pressure measurement accuracy

can be optimized by temporarily stopping all infusions,

then restarting all instruments beginning with instrument

delivering at lowest rate.

Adjustable Pressure Alarm

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

Monitoring Options - Pressure Mode (Continued)

Pressure Baseline

The Pressure Baseline feature, when enabled through the

hospital Data Set profile configuration settings, provides a real-

time bar graph and numeric display of line pressure.

The pressure limit may be reduced if the pressure in the line

is high or changing. This results in the pressure limit being

lowered from the selected setting. If this occurs, first try to

remove or reduce the downstream pressure. Following that,

try to reload the set, wait 15 to 30 seconds and then perform a

Set Pressure Baseline operation. The pressure baseline may

need to be set a second time, after the pressure readings have

stabilized.

For dual channel instruments, select the desired channel as

necessary. The pressure bar graph is not shown when the

split screen display is active.

For optimal results, set the baseline 15 minutes after starting

an infusion. The pressure baseline can be optimized,

particularly at low flow rates (less than 3 mL/h), by resetting

the pressure baseline when the readings are negative.

Check periodically for negative readings; for example, when

programming VTBI. This allows the pressure baseline to

calibrate based on current system pressure.

1. To place channel on hold, press channel’s RUN/HOLD

key. (All infusions connected to channel being base-lined

must be on hold.)

2. Press OPTIONS key.

Manually Setting Pressure Baseline

While Operating in Adjustable Pressure

Mode

OPTIONS

Rate= 125.0 mL/h

VTBI= 1000.0 mL

VI= 0.0 mL

Primary

Limit = 600mmHg

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

96 Dynamic Monitoring System

Monitoring Options - Pressure Mode (Continued)

Pressure Baseline (Continued)

3. Press Set Pressure Baseline soft key. À

Pressure Trend

return

AB OPTIONS

Monitoring Options

Guardrails Library

Set Pressure Baseline

page

• Set Pressure Baseline screen appears.

return

AB OPTIONS

Set

Pressure

Baseline

4. Verify no pressure, due to occlusion or other infusions

through a common line, is present in IV line at this time.

5. For best results, verify set outlet (for example, stopcock) is

located at patient’s heart level before continuing with next

step.

6. Press ok soft key.

return

AB OPTIONS

Set

Pressure

Baseline

OPTIONS

A B

Rate=125.0 mL/h

VTBI=500.0 mL

New

Baseline

Set

Manually Setting Pressure Baseline

While Operating in Adjustable Pressure

Mode (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

Monitoring Options - Pressure Mode (Continued)

Pressure Baseline (Continued)

Manually Setting Pressure Baseline

While Operating in Adjustable Pressure

Mode (Continued)

7. Verify pressure readout is 0 (zero) mmHg. Á

8. To start infusion, press RUN/HOLD key. Â Ã Ä

OPTIONS

Rate= 125.0 mL/h

VTBI=1000.0 mL

VI= 0.0 mL

Primary

0 mmHg

NOTES:

À To return to the normal screen without setting the baseline,

press return soft key.

Á True baseline pressure will be zero or within a few mmHg of

zero. If not, and the pressure is unstable, allow the pressure

to drop to the lowest level and then repeat the Set Pressure

Baseline process.

Â The pressure baseline calibration remains in effect until

the instrument is turned off, the latch is opened, the set is

reloaded, or the set Pressure Baseline function is performed

again.

Ã Setting the manual baseline overrides the auto baseline until

the instrument is turned off, the latch is opened, set is loaded,

or another manual baseline is set.

Ä Setting a manual Pressure Baseline displays a horizontal real-

time bar graph and numeric pressure readings. The vertical

line on the pressure bar graph visually indicates the pressure

alarm limit.

In Pressure Monitoring mode, a trend graph displays monitored

pressure over time. Trend graphs of 15 minutes, 1 hour,

4 hours and 12 hours are available during normal operation

when enabled through the hospital Data Set.

Downstream Occlusions, which occur in Pressure or

Resistance modes, are indicated by a tick mark (y) at the top of

the trend screen.

Pressure Trend Graphs

OPTIONS

A B

return time

clear

PRESSURE

now

-12h

600

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

98 Dynamic Monitoring System

Monitoring Options - Pressure Mode (Continued)

Pressure Trend Graphs (Continued)

Viewing Graphs

1. Dual channel instruments: Select desired channel, as

necessary. Trend graph is not available while split screen

is displayed.

2. Press OPTIONS key.

3. Press Pressure Trend soft key.

OPTIONS

Rate= 125.0 mL/h

VTBI=1000.0 mL

VI= 0.0 mL

Primary

Limit = 300 mmHg

Pressure Trend

return

AB OPTIONS

Monitoring Options

Guardrails Library

Set Pressure Baseline

page

OPTIONS

A B

return time

clear

PRESSURE

now

-12h

600

4. To change graph time frame, press time soft key.

• A solid horizontal line represents current pressure

alarm limit level.

• Gaps in graph may indicate noninfusing conditions;

such as, turned off, on hold, in alarm.

• If channel has been placed in Resistance Monitoring

mode for some portion of a trend graph window,

pressure data is not available and zero values are

plotted.

• A tick mark (y) at top of graph indicates an occlusion. OPTIONS

A B

return time

clear

PRESSURE

now

-12h

600

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

Dynamic Monitoring System

Clearing Graphs

1. To clear graphed data, press clear soft key.

Monitoring Options - Pressure Mode (Continued)

Pressure Trend Graphs (Continued)

OPTIONS

A B

return time

clear

PRESSURE

now

-12h

600

2. Press ok soft key.

• All data is cleared from graphs.

OPTIONS

A B

return ok

All trend data

will be cleared

OPTIONS

A B

return time

clear

PRESSURE

now

-12h

600

Returning to Normal Operating Screen

Press return soft key. OPTIONS

A B

return time

clear

PRESSURE

now

-12h

600

-- Continued Next Page --

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

100 Dynamic Monitoring System

Monitoring Options - Pressure Mode (Continued)

Pressure Trend Graphs (Continued)

OPTIONS

Rate= 125.0 mL/h

VTBI=1000.0 mL

VI= 0.0 mL

Primary

Limit = 200 mmHg

• Normal operating screen appears.

Following events also turn off trend graph:

• Pressing RUN/HOLD key.

• An alarm.

• Dual channel instrument: pressing A B .

• Dual channel instrument: replaced with a split screen

display after 1 minute if both channels are infusing.

Upstream Occlusions Detection

If the flow pathway between the fluid container and the

Pressure Sensor is obstructed due to kinked tubing, a closed

clamp or an improperly installed set, then an OCCLUSION

UPSTREAM condition exists.

Depending on where the upstream path is occluded, flow

may continue for a fraction of a mL before the OCCLUSION

UPSTREAM alarm is produced. At high infusion rates, the

instrument takes relatively little time to alarm. At low infusion

rates, a longer time elapses before the instrument detects the

condition and alarms. In either case, some flow continues

from the instrument during the time prior to the alarm, due to

the elastic behavior of the tubing between the occlusion site

and the pumping mechanism.

If an OCCLUSION UPSTREAM alarm occurs, investigate and

remedy the cause. Ensure that the upstream flow path (such

as tubing) is free of obstructions, that any clamp is open and

that the blue thumb clamp on the Flow Regulator is in the open

(up) position before resuming the infusion.

Returning to Normal Operating Screen

(Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

101

Dynamic Monitoring System

Upstream Occlusions Detection (Continued)

When an upstream occlusion condition is detected:

• OCCLUSION UPSTREAM message appears.

• Audio alarm sounds and infusion stops.

• In certain conditions, upstream alarm system may briefly

pause instrument and present Checking Line message for

10 seconds to confirm or rule out presence of an occlusion.

If occlusion condition is determined not to exist, flow

resumes and no alarm is produced.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

102 Dynamic Monitoring System

THIS PAGE

INTENTIONALLY

LEFT BLANK

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

103

General Set Up and Operation

Audio Adjust

This feature allows the audio volume to be adjusted for alarms,

alerts and KVO tone to either High, Medium or Low if all audio

volume levels are enabled in the Profile configuration or in the

instrument configuration settings and the Profiles features is

set to OFF (not enabled).

1. Press soft key next to lower LCD display.

• Audio volume level displays in the lower LCD display.

Low

Medium

High

• Instrument can be configured to enable only Medium and

High, or only High audio volume levels.

Tamper Resist

Locking and Unlocking Panel Lock

The panel lock feature helps prevent unauthorized changes

to the instrument settings, including turning the instrument off.

The panel lock feature must be set to ON in the hospital Data

Set or in the instrument configuration settings if the Profiles

feature is set to OFF (not enabled). To make changes or

respond to an alarm, the panel lock must be turned off. The

panel lock key ( ) is located behind the handle.

Turning Panel Lock Feature On

Press and hold until appears in lower display.

• Panel Locked appears in Main LCD Display if any other

key is pressed.

GOLD

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

104 General Set Up and Operation

Tamper Resist (Continued)

Locking and Unlocking Panel Lock (Continued)

Turning Panel Lock Feature Off

Press and hold until disappears from lower display.

GOLD

OPTIONS

Panel Locked

VI= 0.0 mL

Rate= 125.0 mL/h

VTBI=1000.0 mL

For dual channel instruments, while panel lock is activated, A

O and A B keys can be used to view settings.

Since panel lock must be inactivated to power down

instrument, it is always off when instrument is powered on.

Turning Panel Lock Feature On (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

105

General Information

Warnings and Cautions

General

WARNINGS

• The SE Pump is designed to stop fluid flow under

alarm conditions. Periodic patient monitoring must

be performed to ensure the infusion is proceeding as

expected. It is a positive displacement delivery system,

capable of developing positive fluid pressures to overcome

widely varying resistances to flow encountered in practice,

including resistances to flow imposed by small gauge

catheters, filters and intra-arterial infusion. It is neither

designed nor intended to detect infiltrations and will not

alarm under infiltration conditions.

• The use of positive displacement infusion devices ported

together with gravity flow infusion systems into a

common IV site may impede the flow of common gravity-

only systems, affecting their performance. Hospital/facility

personnel must ensure the performance of the common IV

site is satisfactory under these circumstances.

• Each time the SE Pump is turned on, verify and/or set

the monitoring mode, resistance alert, and/or pressure

alarm limit. If the monitoring mode, resistance alert,

and/or pressure alarm limit are not verified, the instrument

may not operate within the desired occlusion detection

parameter(s).

• Before each use, verify the pressure or resistance

alarm limits are appropriate for the patient.

• A new alarm or alert reinstates the audio tone.

• Assess patient’s condition before silencing an alarm. Do

not silence alarm if patient safety might be compromised.

• Disconnect from main (AC) and battery power when

performing maintenance.

• To disconnect from main (AC), unplug the power cord

from the back of the instrument.

DANGER

Explosion risk if used in the presence of flammable anesthetic

agents or gases.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

106 General Information

Warnings and Cautions (Continued)

General (Continued)

• Electrical shock hazard. Do not open case. Refer to

qualified service personnel.

WARNINGS

CAUTIONS

• The SE Pump is not intended to replace supervision by

medical personnel. The user must become thoroughly

familiar with the SE Pump features, operation and

accessories prior to use.

• Always use a grounded, three-wire receptacle. Where

the integrity of the protective earth grounding system is in

doubt, operate on internal battery.

• Should an instrument or accessory be dropped or

severely jarred, it should be immediately taken out of use

and inspected by qualified service personnel, to ensure its

proper function prior to reuse.

• If an instrument appears damaged, contact Cardinal

Health for authorization to return it for repair.

Guardrails® Suite MX

WARNINGS

• The Guardrails® Suite MX incorporates dosing limits

and instrument configuration parameters based on

hospital/facility protocol. The software adds a test of

reasonableness to drug programming based on the

limits defined by the hospital/facility. Qualified personnel

must ensure the appropriateness of drug dosing limits,

drug compatibility, and instrument performance, as part

of the overall infusion. Potential hazards include drug

interactions, inaccurate delivery rates and pressure alarms,

and nuisance alarms.

• When delivering an infusion with the Guardrails® Suite

MX protection, ensure the correct profile (for patient

care area) is selected prior to starting an infusion. Failure

to select the appropriate profile could cause serious

consequences.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

107

General Information

Administration Sets

WARNINGS

• When priming:

- Ensure patient is not connected.

- Ensure air is expelled from line prior to beginning

infusion (unexpelled air in line could have serious

consequences).

Failure to prime correctly can delay infusion delivery and

cause the total volume to be infused to read higher than

the actual total delivered to the patient.

• Discard if packaging is not intact or protector caps are

unattached.

• Use only sets dedicated for use with the SE Pump.

The use of any other set may cause improper instrument

operation, resulting in an inaccurate fluid delivery or other

potential hazard.

Warnings and Cautions (Continued)

CAUTION

• Before operating instrument, verify that administration set

is free from kinks and installed correctly in instrument.

Epidural Administration

WARNINGS

• Epidural administration of drugs other than those

indicated for epidural use could result in serious injury to

the patient.

• It is strongly recommended that the source container,

administration set, and SE Pump used for epidural drug

delivery be clearly differentiated from those used for other

types of administration.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

108 General Information

Warnings and Cautions (Continued)

Electromagnetic Compatibility

WARNINGS

• Do not use the SE Pump near Magnetic Resonance

Imaging (MRI).

• Use of any accessory or cable other than those specified

may result in increased emissions or decreased SE Pump

immunity.

• Do not use the SE Pump in a hyperbaric chamber.

Epidural Administration (Continued)

CAUTIONS

• The instrument should not be used adjacent or stacked

with other equipment. If adjacent or stacked use is

necessary, the instrument should be observed to verify

normal operation in the configuration in which it will be

used.

• Portable and Mobile RF communications can affect

Medical Electrical Equipment.

WARNINGS

• The SE Pump can be used for epidural administration of

anesthetic and analgesic drugs. This application is

only appropriate when using anesthetics and analgesics

labeled for continuous epidural administration and

catheters intended specifically for epidural use. Use only

sets dedicated for use with the SE Pump, without a ‘Y’

connector or injection port, for epidural infusions.

- Epidural administration of anesthetic drugs: Use

indwelling catheters specifically indicated for short-term

(96 hours or less) anesthetic epidural drug delivery.

- Epidural administration of analgesic drugs: Use

indwelling catheters specifically indicated for either

short-term or long-term analgesic epidural drug

delivery.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

109

General Information

Battery Management System

The Battery Management System incorporates features which

enhance battery maintenance in order to maximize the life of

the battery, reduce associated costs and increase instrument

availability. The system provides:

• Green : lights when instrument is plugged in.

• Amber : flashes when instrument is operating on battery

power.

• Automatic battery power: if instrument is unplugged or in

the event of a power failure.

• Low battery alert: indicates battery depletion is imminent,

beginning at least 30 minutes prior to a BATTERY

DEPLETED alarm.

Maximum battery capacity, as well as optimal gauge accuracy,

is reached after several complete charge/discharge/recharge

cycles in the refresh process. It is recommended that the

battery be fully charged/discharged/recharged, using the

refresh cycle, before placing the instrument in use. Reference

the Technical Service Manual for detailed information on the

refresh cycle.

Warnings and Cautions (Continued)

Electromagnetic Compatibility (Continued)

CAUTIONS

• The SE pump is intended for use under the supervision of

healthcare professionals only. This is a CISPR 11 Class B

device without the use of the Model 180 (Flow Sensor) and

CISPR 11 Class A when the Model 180 (Flow Sensor) is

used. In a domestic environment, this system may cause

radio interference. Reorienting, relocating or shielding

the system, or filtering the connection to the public mains

network, are examples of steps that can be taken to reduce

or eliminate interference.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

110 General Information

Battery Recharge

The battery recharges whenever the instrument is plugged

into an AC outlet. The battery can be replaced when charging

capacity gets too low.

All batteries gradually lose their capacity to hold a charge

over time and use. To maintain optimal battery performance,

ensure the instrument is connected to AC power whenever

possible, including when it is powered off or stored.

Following certain battery depleted conditions it is necessary

to reset the internal clock so the CQI Reporter data integrity

is maintained (see "Programming", "Programming and

Navigation Tips", "Responding to Time Set Reminder".

Flow Sensor À

The optional flow sensor notifies users of empty containers

and/or upstream occlusions. A handle cap accessory is

available for storing the flow sensor when not in use.

The flow sensor is not used for the first 25 mL delivered when

changing from secondary to primary. This is to account for

overfill of secondary containers.

Battery Management System (Continued)

WARNING

The protective cover over the RS-232

connector must remain in place when

not in use.

Battery Power Gauge and Indicator

The gauge indicates approximate battery run time remaining

under current operating conditions. It is located in the

lower display and is always on. To ensure a more accurate

battery gauge reading, review the remaining battery run time

5 minutes after starting an infusion.

Battery run time may be affected by the operating mode, rate,

monitoring options and back pressure. The gauge accuracy is

based on the last refresh cycle and is affected by the number

of charge/discharge/recharge cycles. The instrument label

and battery gauge are always displayed, even when the

instrument is turned off; however, the battery gauge does not

represent the battery time remaining when the instrument is

turned off.

GOLD

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

111

General Information

Flow Sensor Connectors

Flow Sensor (Continued)

If a flow sensor is not connected to the instrument, ensure

protective plugs are installed at the connector site to prevent

entry of foreign material.

1. Plug a Model 180 Flow Sensor into applicable channel

connector on back of instrument.

CAUTION

Infusing fluids which form smaller

drops, through a 60 drops/mL set,

at high rates may result in a No

Upstream Flow Detected alarm.

This is because the small, rapidly

falling drops form a continuous

stream which does not trigger the

flow sensor. In this event, unplug the

flow sensor from the instrument.

2. Attach flow sensor to upper portion of drip chamber.

• When using flow sensor, correct placement is essential

for proper operation. Some administration set drip

chambers have a flange at top to which flow sensor

can be attached. Attachment on flange ensures

proper placement.

Upper surface of flow sensor should be slightly below

drop-forming orifice but above level of fluid in drip

chamber.

Ensure drip chamber is at least 2/3 full and sensor

optics are clean. Fluid level in drip chamber must be

checked/re–established after each empty container

condition

• When using flow sensor option while ambulating

or transporting a patient from one area to another,

use care to avoid excessive swinging of solution

container(s).

3. Attach flow sensor to instrument handle when not in use.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

112 General Information

Alerts Counter À

The instrument keeps a running count of Guardrails® Alerts

that occur. This information may be viewed with the Alerts

Counter feature.

Definitions Á

GR Alerts: Total number of Hard Limit and Soft Limit

Guardrails® alerts that occur.

GR Starts: Total starts when a Guardrails® drug or

Guardrails® fluid is selected. GR Start counter

also increments if a rate or dose rate change

occurs during a running infusion. A transition to

KVO rate is not counted as a start.

Log % Full: CQI log retained by instrument can hold up

to 300 Guardrails® alerts and resolutions

snapshots. The % full indication represents

percentage of 300 available logged snapshots

used. For example, if log currently contains 30

snapshots, % full indication is 10%. Log always

retains most recent 300 snapshots, therefore,

even if this indication is 100% full, subsequent

Guardrails® alerts and resolution snapshots

are stored and oldest ones are deleted to make

space for newer ones.

CAUTION

Do not use solvents or cleaning

agents. Damage to plastic parts of

the flow sensor could occur.

NOTE:

À If the flow sensor option is in use, VTBI can be turned off by

selecting VTBI, pressing CLEAR and then ENTER keys.

Primary VTBI can be deleted from the primary mode setup

page (see “General Information, System Conﬁ gurable

Options”).

Flow Sensor (Continued)

4. Routinely clean flow sensor with warm water while

actuating slider, then dry thoroughly.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

113

General Information

Viewing Alerts Counter

1. Press OPTIONS key.

2. Press Alerts Counters soft key.

3. To return to main display, press return soft key.

To clear counter (reset all values to zero), press clear soft

key.

To view second event counter page, press page soft key.

• Last cleared date displays.

Alerts Counter (Continued)

Definitions (Continued)

New Patients: Total number of new patients or profiles

selected. Counter increments when yes to New

Patient? screen prompt or a different profile at

instrument power up is selected.

Overrides: Total number of Soft Limit Guardrails® alerts

that are overridden. Counter increments when

yes is selected in response to soft override alert

prompt.

Soft Alerts: Total number of Soft Limit Guardrails® alerts that

occur. Counter increments when either yes or

no is selected in response to soft override alert

prompt.

Total Starts: Total number of infusion starts. A start occurs

when run key is selected from an inactive or

paused condition.

NOTES:

À For dual channel instruments, the counters represent the total

counts for both channels.

Á These are the counter labels as they appear on the Main

Display.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

114 General Information

Nurse Call (7130/7230 Only)

Activating Nurse Call Feature

If the instrument is equipped with the optional nurse call

feature, alarms and some alerts from the instrument are

relayed to the hospital’s existing nurse call system. No

instrument operating features are changed. The instrument

alarms with or without the nurse call installed.

1. Plug nurse call cable into

RS 232

on instrument back

panel. À

2. Press channel’s POWER key.

• Instrument beeps briefly to signal proper operation.

3. Plug nurse call cable into nurse call system.

4. Operate instrument as described in this document. Á Â

NOTES:

À A false remote alarm may occur if the nurse call plug is not

properly inserted.

Á All alarms and some alerts activate the nurse call system.

The following alerts will not activate the nurse call system:

Checking Line, Load Dose Complete, Secondary Complete.

Â Disconnecting the nurse call cable from the wall or

turning off the instrument activates the nurse call system.

Disconnecting the nurse call cable from the instrument

will not activate the nurse call system.

If an Alarm Occurs

1. Determine cause and appropriate corrective action (see

"Troubleshooting and Maintenance", “Alarms, Alerts,

Prompts”).

2. Reset nurse call system, as required.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

115

General Information

Pole Clamp

The uniquely designed pole clamp adapts to a wide variety

of surfaces (such as, poles, bed rails) to provide greater

versatility and to simplify transports.À Á It features:

• 360º rotation in 90º increments

• ergonomically designed knob

• accommodates diameters from 15 to 35 millimeters

NOTES:

À The illustrated pole clamp knob may not reflect the knob in

use on the instrument.

Á When using multiple instruments, care should be taken to

evenly distribute the instruments to ensure stability.

WARNING

To ensure proper occlusion

detection, DO NOT operate the

instrument tilted back more than 45º

from the upright position.

Changing Pole Clamp Orientation À

1. Press and hold rotation lever.

Lever

NOTE:

À The illustrated pole clamp knob may not reflect the knob in

use on the instrument.

2. Reposition clamp.

3. Release lever at desired position.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

116 General Information

RS-232 Computer Link

The optional Computer Link feature allows a hospital/facility

computer to interact with the instrument. The computer cannot

start or stop the instrument, set the rate, or make any change

in status. The feature may be enabled or disabled by qualified

personnel in the instrument configuration settings. If the

feature is enabled (On) the user may select Monitor, to allow

the computer to receive information from the instrument, or

Off. When Off is selected, the computer cannot communicate

with the instrument.

To assure continued electromagnetic compatibility

performance, the communications cable attached to the

instrument should be no longer than 1 meter, have fully

shielded connector housings, and have a 100% coverage

braid/foil shield attached to the connector housings around the

signal conductors with the cable jacket.

Connecting to a Computer

1. Press OPTIONS key.

2. To advance to next page, press page soft key.

3. Press Computer Link soft key.

4. Press Monitor soft key.

5. Press ok soft key.

6. Connect an RS-232 cable from hospital computer to

RS 232

port on instrument back panel.

• During communication between host computer and

instrument, MNTR (Monitor Mode) appears in lower

LCD. À

• If communication is interrupted, MNTR flashes for 60

seconds.

MNTR

GOLD

NOTE:

À MNTR remains in the lower display once the mode is selected

and communication with the computer has been established.

WARNINGS

• Use of any accessory or cable

other than those specified may

result in increased emissions or

decreased SE Pump immunity.

• The protective cover over the

RS-232 connector must remain

in place when not in use.

• Only equipment that complies

with IEC EN 60601-1 or UL

1069 (approved medical or

hospital signaling equipment)

should be connected to the RS-

232 connector.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

117

General Information

RS-232 Computer Link (Continued)

Disconnecting from a Computer

1. Press OPTIONS key.

2. To advance to next page, press page soft key.

3. Press Computer Link soft key.

4. Press Off soft key.

5. Press ok soft key.

6. Disconnect RS-232 cable from

RS 232

port on instrument

back panel.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

118 General Information

Features and Displays

Operating Features, Controls, Indicators

Models 7130/7131

SEC

PRI

Clear Enter

OPT PRI HLD SEC KVO

RUN

HOLD

POWER

OPTIONS

456

789

ml/hr

Power Key: Turns instrument on and

off.

Power Indicator:

Green = Plugged in and charging.

Flashing Amber = Battery power.

Infusing Indicator: Indicates

instrument is infusing.

Alarm Indicator: Indicates instrument

is in alarm and has stopped infusing.

RUN/HOLD Key: Starts and stops

infusion.

OPTIONS Key: Accesses additional

features.

Secondary (SEC) Key: Selects

secondary mode.

Primary (PRI) Key: Selects primary

mode.

Soft Keys: Reference “Programming

and Navigation Tips”.

ENTER Key: Accepts value or

selection entered.

Silence Key: Silences audible alarm or

alert for 2 minutes; message remains on

screen. New alarm or alert reinstates

audible tone.

CLEAR Key: Clears selected numeric

value.

Audio Volume Key: Sets audio volume

for alarms, alerts and KVO tone. Press

key to adjust volume.

Numeric Keypad: Enters/changes

values.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

119

General Information

Features and Displays (Continued)

Operating Features, Controls, Indicators (Continued)

Channel Select Keys/Indicators:

Select channel A or B. Light to indicate

which channel is selected.

Alarm Indicators: Indicate a channel

is in alarm and has stopped infusing.

Infusing Indicators: Indicate a

channel is infusing.

RUN/HOLD Keys: Start and stop

infusion on selected channel. To restart,

channel must be selected.

Power Indicator:

Green = Plugged in and charging.

Flashing Amber = Battery power.

Power Keys: Turn channels on and off.

OPTIONS Key: Accesses additional

features.

Secondary (SEC) Key: Selects

secondary mode.

Soft Keys: Reference “Programming

and Navigation Tips”.

ENTER Key: Accepts value or

selection entered.

Silence Key: Silences audible alarm or

alert for 2 minutes; message remains on

screen. New alarm or alert reinstates

audible tone.

CLEAR Key: Clears selected numeric

value.

Audio Volume Key: Sets audio volume

for alarms, alerts and KVO tone. Press

key to adjust volume.

Numeric Keypad: Enters/changes

values.

OPTIONS

SEC

PRI

POWER

RUN

HOLD

Clear Enter

PRI SEC HLD OPT KVO

HLD PRI SECKVO OPT

456

789

•0

POWER

RUN

HOLD

A B

ml/hr ml/hr

Models 7230/7231

Primary (PRI) Key:

Selects primary mode.

Channel must be

selected.

Split Screen Key:

Displays information for

both channels when both

channels are infusing.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

120 General Information

OPTIONS

SEC

PRI

POWER

RUN

HOLD

Clear Enter

PRI SEC HLD OPT KVO

HLD PRI SECKVO OPT

456

789

•0

POWER

RUN

HOLD

A B

ml/hrml/hr

Features and Displays (Continued)

Operating Features, Controls, Indicators (Continued)

Panel Lock Key

RS-232 Connector Cover

Flow Sensor Receptacle(s)

RS-232 Connector

Pole Clamp Rotation Lever

Battery Door

Potential Equalization Connector

(7131/7231)

Latch

Flow Control Actuator

Clamp Arms

Pumping Mechanism

Loading Guide

Pressure Transducer

Air-in-Line Detector

Air-in-Line Arm

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

121

General Information

LED rate display is easily viewed from a distance.

Rate Display

Indicates current infusion rate(s) in mL/h. Flashes to indicate

hold or alarm condition, and when in KVO mode.

Model 7130/7131 Status bar

Indicates which mode instrument is in: Optional Modes,

Primary, Hold, Secondary, or KVO.

Model 7230/7231 Status bar

Indicates which mode each channel is in: KVO, Optional

Modes, Hold, Primary, or Secondary.

Features and Displays (Continued)

Displays

Main Display

The Main Display is backlit for easy viewing. The backlight

dims when operating on battery power as an energy-saving

feature. Pressing any key automatically turns the backlight up

again.

CAUTION

Appearance of lines and/or dots

that remain on constantly when

the instrument is powered on may

indicate improper functioning of

the Main Display. Although the

instrument is functioning properly,

return it to qualified service

personnel.

Rate Display

KVOOPT HLD SEC

PRI

ml/hr

KVO OPT HLD SECPRI

ml/hr ml/hr

PRI SEC HLD KVOOPT

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

122 General Information

Features and Displays (Continued)

Displays (Continued)

Lower Display

The lower LCD display is backlit for easy viewing. The display

dims when operating on battery power, as an energy-saving

feature.

Panel Lock Indicator

Displayed if panel lock is on.

Audio Volume Indicator

Indicates audio volume for alarms and alerts.

Computer Mode Indicator

Displayed if instrument is in computer monitor mode.

Instrument ID Label

Characters are entered to identify selected Profile or

configuration, ownership, location, etc.

Battery Power Gauge

Indicates approximate battery time remaining under current

infusing conditions.

MNTR

GOLD

Feature Definitions

Bolus Dose Continuous infusions within Dose Rate Calculator mode may include Bolus

dosing. Enabling this mode allows a bolus infusion to be programmed using

either Drug Library or Drug? NO DOSE LIMIT option. Bolus infusion can be

programmed with or without a continuous infusion to follow bolus.

Data Set Created using Editor Software authoring tool and then transferred to SE

Pump. A Data Set reflects facility’s best-practice guidelines for IV Drug

administration and includes: Profile Drug Libraries, Profile Fluid Libraries,

Clinical Advisories and instrument configurations.

Drug Library Allows flow rate or drug dose rate to be entered for a continuous infusion.

System then calculates alternate parameter based on drug concentration and

weight if used.

Guardrails® Suite MX Designed to help prevent programming errors by:

• Customizing instrument configurable settings to meet need of selected

hospital/facility area/unit (profile).

• Comparing user programming with hospital-defined best-practice

guidelines.

• Providing a prompt if an out-of-limits entry is made.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

123

General Information

Configurable Settings

With the Profiles feature enabled, the settings are configured

independently for each profile. A hospital-defined, best-

practice Data Set must be uploaded to enable the Profiles

feature.

If the Profiles feature is not enabled (off) or if no Data Set is

loaded, the configurations options are set in the configuration

mode by qualified service personnel. If the configuration

settings need to be changed from the factory default settings,

reference the Technical Service Manual or contact Cardinal

Health Technical Support for technical, troubleshooting, and

preventive maintenance information.

Features and Displays (Continued)

Feature Definitions (Continued)

IV Fluid Allows rate and volume to be entered for an infusion that is delivered in mL/h,

providing a prompt if a rate is entered that is outside facility’s best-practice

guidelines.

Profile A unique set of system configuration settings and best-practice guidelines

for a specific patient population or patient type, and can consist of following

components:

• Instrument configuration settings.

• A Drug Library, which includes Guardrails® drug names, standard

concentrations, dosing units, duration limits, and optional associated

Clinical Advisories for continuous, intermittent and bolus dose infusions.

• An IV Fluid library, an optional library consisting of IV fluids (for example,

TPN) and limits around rate of delivery.

Profile settings are established by facility’s own multi-disciplinary team prior

to system implementation. Profile parameters are used to create a Data

Set, which is then transferred to SE Pump.

Directions

Ala

SE Pump

Models 7130

7131

7230

7231

124

eneral In

ormation

Configurable Settings (Continued)

Configurable Option Definitions - General

n L

ne:

Air in Line Threshold

(

microliters

)

Sets upper limit for a sin

le bolus of air to pass without alarm.

n other words, it is amount of air allowed to pass through air

n-line detector be

ore an air-in-line alarm sounds.

ne o

different air-in-line detection settings can be selected: 50, 100,

200,

mcL

AIL A

ccu

ator

Detects presence of multiple air bubbles that are too small to

etecte

AIL

etect

ccumu

ato

feature, when enabled, looks for 10-15% of downstream fluid

ath to be air be

ore

ivin

an A

UMULATED AIR IN LINE

alarm. Volume of air that tri

s accumulated air detection alarm

aries based on current settin

or sin

le air bolus.

AIL R

eset

Allows clinician to res

ond to an air-in-line alarm, assess its

linical si

icance, and choose whether or not to continue

nfusion without removing air. Reset feature allows only current

bubble to proceed without trippin

alarm.

Aud

rans

rov

es an au

dibl

e tone w

en secon

ary

VTBI

reac

es zero, to

cate

usion has transitioned to primar

rate

Provides clinician with ability to adjust audio volume for alarms, alerts

and KV

tone to either Hi

h, Medium, or Low i

all audio volume levels

are enabled. Audio volume indicator in lower LCD display indicates audio

olume selected. Instrument can be con

ured to enable onl

Medium

and High, or only High audio volume levels if desired

econdary to Primary)

uration Nam

llows a 4-di

it instrument ID label to appear in lower L

D displa

, identi

atient care

rofile.

(Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

125

General Information

Configurable Settings (Continued)

Configurable Option Definitions - General (Continued)

Dynamic Monitoring:

Auto Restart Plus Part of the Dynamic Monitoring system and designed to help minimize

nuisance “occlusion downstream” alarms. It allows instrument to

automatically continue an infusion following detection of a downstream

occlusion if downstream pressure falls to an acceptable level within a 40-

second Checking Line period. May be set to off (0 restarts) or to allow from

1 – 9 Checking Line restarts. If allowable number of restarts is exceeded, or

when resistance or pressure conditions indicate an occlusion, an occlusion

downstream alarm occurs.

Monitoring Options Dynamic monitoring provides clinician ability to select one of following

monitoring modes: Resistance mode, High Resistance mode or Pressure

mode. All of these modes offer an optional Auto-Restart Plus feature and

optional trend graph display.

Trends Provides ability to display downstream pressure or flow resistance over time.

Trend graphs of 15 minutes, 1 hour, 4 hours and 12 hours are available during

normal operation. When Trends is enabled, if instrument is operating in

pressure mode, a pressure trend graph is available, and when it is operating

in resistance mode, a resistance trend graph is available.

Dynamic Monitoring - Pressure:

Adjustable pressure is designed to monitor IV line/site pressure and provide user-adjustable pressure

alarm limits. It is used for Precision Flow mode or for high resistance systems; such as, infusion

through transducers, into dialysis systems and through highest resistance catheters. Pressure mode

may be configured to operate with a fixed pressure alarm limit threshold so that it is not user-adjustable.

Manual Pressure Baseline Provides a real-time bar graph and numeric display of line pressure.

Pressure Alarm When Pressure Display is enabled, Pressure Alarm may be set to

Adjustable Pressure mode or Fixed Pressure mode.

Pressure Display In Adjustable Pressure monitoring mode, pressure alarm limit may

be varied by from 25 mmHg to maximum configured pressure limit in

25 mmHg increments. Pressure Display indicates current pressure

limit and provides ability to adjust limit by pressing “increase” or

“decrease” arrows.

In Fixed Pressure mode, pressure limit of 600 mmHg displays,

with no means of adjusting it. When Pressure Display is disabled,

instrument automatically defaults to Fixed Pressure mode.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

126 General Information

Configurable Settings (Continued)

Configurable Option Definitions - General (Continued)

Dynamic Monitoring - Pressure:

(Continued)

Pressure Limit, Initial This is default pressure alarm limit that is automatically set when

instrument is powered on and a new profile is selected or New

Patient? - Yes is selected. Alarm level must be less than or equal to

maximum pressure limit.

Pressure Limit, Maximum In Adjustable Pressure monitoring mode, pressure alarm limit may be

varied by from 25 mmHg to this maximum configured pressure limit in

25 mmHg increments. A value that exceeds this pressure limit cannot

be selected.

Dynamic Monitoring - Resistance:

Resistance Monitoring eliminates the impact of patient elevation and flow rate, to provide the most direct

assessment of patency. It is designed to monitor IV line/site resistance providing optimum sensitivity

for most IV applications. High Resistance is designed to monitor IV line/site resistance with optimum

sensitivity where higher resistance catheters are used.

Default Resistance Alert Default resistance alert level that is automatically set when instrument

is powered on and a new profile is selected or New Patient? - Yes is

selected. Resistance Alert Marker can be adjusted up or down from

this default setting, as needed.

Resistance Alert Provides an early warning of increasing flow resistance. When

enabled, Resistance Alert marker can be set by from 0% to 100% of

scale in 5% increments (Resistance Display must also be enabled).

To optimize alert feature, it is advisable to set alert level 20-30%

higher than initial displayed resistance, which should be read

approximately 2 minutes after starting an infusion.

Resistance Display When enabled provides a bar graph on Main Display to indicate

current % resistance on a scale of 0 – 100%. When disabled,

resistance alert feature is unavailable.

Resistance Pressure Setting Provides an “Occlusion Downstream” alarm when measured pressure

reaches Resistance Pressure limit while operating in Resistance

Mode. This threshold may be set from 1 to 600 mmHg in 1 mmHg

increments. In other words, while operating in Resistance mode or

High Resistance mode, an “Occlusion Downstream” condition can be

detected in 2 ways; measured resistance reaches 100% of scale or

configured Resistance Pressure Setting is exceeded.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

127

General Information

KVO Rate

KVO (keep vein open) mode automatically occurs when primary VTBI has

counted down to 0.0 mL. Channel switches to preset KVO rate or remains at

current rate, whichever is less. KVO rate may be set to a value between 0.1 and

20 mL/h in 0.1 mL/h increments. KVO rate is not adjustable by the clinician.

Configurable Settings (Continued)

Configurable Option Definitions - General (Continued)

Optional Modes:

Optional modes include Loading Dose, Dose Rate Calculator, Multi-Step, and Multi-Dose. Each of

these can be either enabled or disabled. When disabled, they will not appear on the Options menu and

cannot be accessed by the clinician.

Dose Rate Calculator Allows clinician to enter either flow rate or drug dose rate for a continuous

infusion. System then calculates alternate parameter based on drug

concentration and weight if used.

For an intermittent infusion, system calculates total dose based on drug

amount and patient weight (kg) or BSA (m2) if used. Next, clinician enters

either volume and time to calculate rate, or rate and volume to calculate

time.

Dose rate calculator must be enabled in order to access Bolus Dose feature

and Drug Library.

Loading Dose Allows clinician to set up an initial infusion rate for a specific volume, to

be followed automatically by a maintenance rate (primary settings) from

same container. This is useful for delivering fluid challenges. Limits do

not apply when using Loading Dose feature. To deliver a loading dose of a

medication selected from Drug Library, Bolus Dose feature may be used.

Multi-Dose Allows 1 - 24 doses to be programmed at equally spaced intervals on same

instrument over a 24-hour period. This mode allows delivery of multiple,

equal doses from same IV container at regularly scheduled intervals. Limits

do not apply when using Multi-Dose feature. Within this mode, a delayed

start option allows instrument to be programmed to delay infusion start for

up to 8 hours.

Multi-Dose Alert When enabled, this feature alerts clinician of completion of each dose

delivered during a Multi-Dose program.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

128 General Information

Configurable Settings (Continued)

Configurable Option Definitions - General (Continued)

Optional Modes: (Continued)

Multi-Step Allows a sequential drug delivery program (up to 9 steps) to be set

delivering volumes of fluid at different rates at each step. This allows

instrument parameters to be set up once and deliver a step profile,

eliminating need to change rate and VTBI after each step of infusion.

Infusion may be programmed in rate/volume or volume/time. Limits do not

apply when using Multi-Step feature.

Rate, Maximum

Maximum infusion rate may be set to a value from 0.1 to 999.9 mL/h in 0.1 mL/h

increments.

Configurable Option Definitions - Guardrails® Suite MX

BSA, Maximum Sets maximum patient body surface area for each profile. May be set to a

value from 0.05 to 3 m2 (meters squared) in 0.01 m2 increments.

Dose Checking Mode Dose Checking (limit checking) has 2 selectable options:

• Always checking option causes a Guardrails® alert to occur each time

a dose limit is exceeded. If limit is overridden, drug label displays an

indicator (↑↑↑ or ↓↓↓ arrows) that infusion is beyond current Soft Limit.

• Smart option causes an initial Guardrails® alert to occur when a dose

limit is exceeded. Subsequent programming beyond dose limit does

not cause an alert to display. If limit is overridden, drug label displays

an indicator (↑↑↑ or ↓↓↓ arrows) that infusion is beyond current Soft

Limit

Weight, Maximum Sets maximum patient weight (kg) for each profile. May be set to a value

from 0 to 4534 kg in 1 kg increments.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

129

General Information

Configurable Options

Configurable Settings (Continued)

* These features are configured only within a hospital-defined best-practice Data Set.

Feature Options Default

Air-in-Line:

Air-in-Line Accumulator

Air-in-Line Threshold

Air-in-Line Reset

On/Off

50,100,200, or 500 mcL

On/Off

100 mcL

Off

Audio:

Transition Tone

Volumes

On/Off

Low/Med/Hi Med/Hi Hi

Low/Med/Hi

Configuration Name 4 alphanumeric characters GOLD

BSA, Maximum* 0.05 - 3 3

Dynamic Monitoring:

Auto Restart Plus

Monitoring Options

Trends

0 (Off) /1 to 9

Resistance/High Resistance/Pressure

On/Off

Pressure

Pressure:

Manual Pressure Baseline

Pressure Alarm

Pressure Display

Pressure Limit, Initial

(Configuration Mode: Def Alarm)

Pressure Limit, Maximum

On/Off

Adjustable/Fixed

On/Off

25-600 mmHg

25-600 mmHg/600 mmHg

Adjustable

600 mmHg

Resistance:

Default Resistance Alert

Resistance Alert

Resistance Display

Resistance Pressure Setting

0-100%

On/Off

1-600 mmHg

100%

600 mmHg

Dose Checking Mode* Smart/Always Always

KVO Rate 0.1 - 20 mL/h 5.0 mL/h

Optional Modes:

Bolus

Dose Rate Calculator

Loading Dose

Multi-Dose

Multi Dose Alert

Multi-Step

On/Off

Off

Panel Lock On/Off On

Rate, Maximum 0.1 - 999.9 mL/h 999.9 mL/h

Weight, Maximum* 0.001 - 4,534 kg 4,534 kg

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

130 General Information

System Configurable Options

The following features can be customized by qualified service personnel in the Configuration or

Diagnostic Modes.

Configurable Settings (Continued)

Feature Options Default

Computer Link:

Baud Rate

Mode

Parity

300/600/1200/1800/2400/4800/9600

Monitor/Off, Off

Even/Odd/None

9600

Off

None

Instrument ID* 9 digits 000000000

Maintenance:*

Maintenance Interval

Maintenance Reminder

1-52 wks

On/Off

52 wks

Pressure Sensor*

Self Check Interval 1-52 wks 12 wks

Profiles On/Off Off

Regional Settings Region: North America, European

Language: English North America English **

VTBI On/Off (Flow Sensor use) On

* These features are configured in the Diagnostics Mode.

** Instruments manufactured for sale in Europe will be set, at the factory, to European English. If a new

logic board is installed or the instrument is set to factory defaults, the instrument defaults to North

America English. If the language needs to be reset, contact qualified service personnel.

Specifications

Administration Sets: Use only administration sets for SE Pump.

Alarms: Accumulated Air In Line Key Stuck

Air In Line Latch Open

Battery Depleted No Upstream Flow Detected

Channel Malfunction Occlusion Downstream

Computer Link Failure Occlusion Upstream

Flow Sensor Unplugged Primary Flow Detected During Secondary

Hold Time Exceeded Set Out

Instrument Malfunction Set Up Time Exceeded

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

131

General Information

Battery: Rechargeable nickel-cadmium. A single channel instrument operates

for 4 hours nominal and a dual channel instrument operates for 3 hours

nominal, under following conditions:

• new, fully charged battery

• ambient room temperature, 73±7°F (23±4°C)

• resistance monitoring modes

• rate: 100 mL/h on a single channel instrument and 50 mL/h on each

channel of a dual channel instrument

Battery run time is affected by operating mode, rate, monitoring options

and back pressure (see "General Information", “Battery Management

System”).

Case: Impact and flame resistant plastic.

Critical Volume: Maximum incremental volume in case of single point failure does not

exceed 1.0 mL at 999.9 mL/h.

Dimensions: (Nominal) 7130/7131 7230/7231

Depth* 5.0 in/12.7 cm 5.0 in/12.7 cm

Height 8.6 in/21.8 cm 8.6 in/21.8 cm

Power Cord 10 ft/3 m 10 ft/3 m

Weight** 6.6 lb/3.0 kg 8.4 lb/3.8 kg

Width 7.6 in/19.3 cm 10.7 in/26.7 cm

* Without pole clamp. ** Without power cord.

Downstream Occlusion: À

Time to Alarm

When occlusion alarm pressure limit is set to maximum threshold setting,

maximum infusion pressure generated into a hard occlusion at 25 mL/h is

11.6±3.9 psi.

Specifications (Continued)

Maximum 2 75 2 7

Typical 0.6 30 0.6 4

Maximum 1 25 1 3

Typical 0.1 1 0.1 1

Monitoring Options

Time to Detect

Downstream Occlusion

(minutes)

Threshold Settings

1 mL/h

25 mL/h

Pressure Resistance and

High Resistance

100%

600 mmHg

100%

25 mmHg

mmHg

600

mmHg

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

132 General Information

Specifications (Continued)

Downstream Occlusion: À (Continued)

Bolus Volume

Testing performed using Model 72003 administration set, at 68±8°F

(20±4°C).

Environmental Conditions: Operating Storage

Atmospheric Pressure 700 to 1060 hPa 500 to 1060 hPa

Relative Humidity 20 to 90% 5 to 95%

Noncondensing Noncondensing

Temperature Range 41 to 104°F -40 to 140°F

(5 to 40°C) (-40 to 60°C)

Flow Rate Range: 0.1 to 600.0 mL/h in 0.1 mL/h increments (secondary mode)

0.1 to 999.9 mL/h in 0.1 mL/h increments (all other modes)

Ground Current Leakage: Electrical leakage current, enclosure: <100 microamperes

Electrical leakage current, patient: <10 microamperes

KVO Flow Range: 0.1 to 20.0 mL/h in 0.1 mL/h increments

Mode of Operation: Continuous

Power Requirements: 100-240 V~, 50/60 HZ (72 VA MAX), 3-wire grounded system

Class 1 with Internal Power Source

Maximum 0.5 0.5 0.5 0.5

Typical <0.1 0.3 <0.1 <0.1

Maximum 0.5 0.5 0.5 0.5

Typical <0.1 0.3 <0.1 0.3

Monitoring Options

Bolus Volume Released

Upon Correcting

Downstream Occlusion

(mL)

Threshold Settings

1 mL/h

25 mL/h

Pressure Resistance and

High Resistance

100%

600 mmHg

100%

25 mmHg

mmHg

600

mmHg

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

133

General Information

Specifications (Continued)

Rate Accuracy: For rates greater than 1 mL/h, up to 999.9 mL/h: ±5%, 95% of time with

95% confidence, under conditions listed below.

For rates equal to or less than 1 mL/h: ±6.5%, 95% of time with 95%

confidence, under conditions listed below.

Rate Accuracy Test Conditions:

Infusion rate range: 0.1 to 999.9 mL/h

Head height: 24 ±1 in. (61±2.5 cm)

Test solution: distilled water

Environment temperature: 68±8°F (20±4°C)

Back pressure: 0 psi

Needle: 18 gauge

Set Model: 72003

Minimum collection volume: 6 mL

Volume Infused Range: 0.0 to 9999.9 mL in 0.1 mL increments

VTBI Range: 0.1 to 9999.9 mL in 0.1 mL increments (Basic Infusion, Drug Library

Primary Infusion, IV Fluid Infusion and Multi-Step mode); 0.1 to 999.9 mL

in 0.1 mL increments (all other modes)

NOTE:

À Time to Occlusion and Bolus Volume data tested to standards defined in AAMI ID26:1998, Section

51.101 b.

CAUTION

Variations of head height, back pressure, time, monitoring mode option,

pump tilt or any combination of these may affect rate accuracy. Factors

that can influence head height and back pressure are: Administration set

configuration, IV solution viscosity, and IV solution temperature. Back

pressure may also be affected by catheter type. See "Trumpet and Start-

up Curves" for data on how certain factors influence rate accuracy.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

134 General Information

Symbols and Terms

MM-YYYY

IPX1

Alarm indicator.

Caution: Refer to accompanying documentation.

Audio volume.

Approximate battery time remaining under current infusing conditions. Battery gauge does

not represent battery time remaining when instrument is turned off.

Conformité Européenne [CE - Marking] notified body “0086”: British Standards Institution.

Electrical shock protection rating: Type CF À

Type CF defibrillation-proof equipment. À

Explosion risk if used in presence of flammable anesthetics.

Flow sensor receptacle (optional), channel A.

Flow sensor receptacle (optional), channel B.

Infusing indicator.

Indicates degree of protection, liquid ingress.

Manufacturing Date: Number adjacent to symbol indicates month and year of

manufacture.

Nurse Call (optional for 7130/7230).

Consult operating instructions.

Panel lock.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

135

General Information

Symbols and Terms (Continued)

Green = instrument plugged into AC power and battery being charged.

Flashing amber = instrument running on battery power and battery being depleted.

RS-232 connector.

Silence mode.

Split screen (dual channel instrument only).

A brief tone during transition from one mode to another.

Canadian and U.S. Certification Mark: Products bearing this mark have been tested

and certified in accordance with applicable U.S. and Canadian electrical safety and

performance standards (CSA C22.2 No. 125).

Single-Use. Do not re-use.

DEHP in fluid pathway.

No DEHP in fluid pathway.

Product contains latex.

Product is latex free.

Drops per milliliter specification for product is identified on drop symbol.

Product incorporates Needle-Free Valve ports and should not be accessed by a

needle.

Approximate set priming volume.

Expiration date for product is identified near hour glass symbol.

Do not use if package is damaged.

Transition Tone

A B

RS 232

Single-Use

DEHP

LATEX

»XX ml

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

136 General Information

Symbols and Terms (Continued)

cm centimeter

day day (d)

gm gram (g)

h hour

HLD infusion in “hold” mode

in inch

kg kilogram

KVO “keep vein open” infusion rate mode

lb pound

mcg microgram (μg)

mcL microliter (μL)

mEq milliequivalent

mg milligram

min minute

mL milliliter

mmol millimole

mUn milliunit

nan nanogram (ng)

OPT optional mode

PRI primary infusion mode

rev revolution (r)

SEC secondary infusion mode

Un unit

VI volume infused

VTBI volume to be infused

wks weeks

NOTE:

À Depending on manufacturing and distribution timing, the SE Pump may bear either the CF or

CF Defibrillator-Proof symbol on the main rating label. The SE Pump has been tested and

complies with IEC 60601-1 Amendment 2, Clause 17 (h) for Defibrillator-Proof Equipment.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

137

General Information

Trumpet and Start-Up Curves

DESCRIPTION AND EXPLANATION OF TRUMPET

AND START-UP CURVES

In this instrument, as with all infusion systems,

the action of the pumping mechanism and

variations in individual administration sets cause

short-term fluctuations in rate accuracy. The

following graphs show typical performance of the

system for both Pressure and Resistance modes

in two ways:

• Accuracy during various time periods over

which fluid delivery is measured (trumpet

curves).

• Delay in onset of fluid flow when infusion

commences (start-up curves).

Product operation is not affected by the selection

of Resistance or High Resistance at 0.1, 1.0, and

25 mL/h; therefore, High Resistance graphs are

not included.

Trumpet curves are named for their characteristic

shape. They display discrete accuracy data

averaged over particular time periods or

“observation windows”, not continuous data

versus operating time. Over long observation

windows, short-term fluctuations have little

effect on accuracy, as represented by the flat

part of the curve. As the observation window is

reduced, short-term fluctuations have greater

effect, as represented by the “mouth” of the

trumpet. Knowledge of system accuracy over

vari ous observation windows may be of interest

when certain drugs are being administered.

Because the clinical impact of short-term

fluctuations on rate accuracy depends on the

half-life of the drug be ing infused and on the

degree of intravascular integration, the clinical

effect cannot be determined from the trumpet

curves alone. Knowledge of the start-up

characteristics should also be considered.

The start-up curves represent continuous flow

rate versus operating time for two hours from the

start of the infusion. They exhibit the delay in

onset of delivery due to mechanical compliance

and provide a visual representation of uniformity.

Trumpet curves are derived from the second

hour of this data.

FLOW CHARACTERISTICS UNDER VARYING

DELIVERY CONDITIONS

Effects of Pressure Variations

Under conditions of +100 mmHg pressure, the

SE Pump typically exhibits a long-term accuracy

offset of approximately -1.4% from mean values.

Under conditions of +300 mmHg pressure, the

SE Pump typically exhibits a long-term accuracy

offset of approximately -1.5% from mean values.

Under conditions of -100 mmHg pressure, the

SE Pump typically exhibits a long-term accuracy

offset of approximately -0.8% from mean values.

Resulting trumpet observation points typically

track those of accuracy; therefore, no significant

change in short–term variations result under

these pressure conditions.

Effects of Negative Solution Container Heights

With a negative head height of -0.5 meters, the

SE Pump typically exhibits a long–term accuracy

offset of approximately -5.8% from mean values.

Resulting trumpet observation points typically

track those of accuracy; therefore, no significant

change in short–term variations result under

negative head height conditions.

Effects of Rate

For applications where flow uniformity is a

concern, use of the Pressure Mode at rates of

1.0 mL/h or above is recommended.

NOTE: Tests conducted in accordance with

IEC 60601–2–24, “Particular requirements for

safety of infusion pumps and controllers” and

AAMI ID26–1998 “Medical electrical equipment

- Part 2: Particular requirements for the safety

of infusion pumps and controllers”, using a

Model 72003 Administration Set (includes Flow

Regulator).

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

138 General Information

Trumpet and Start-Up Curves (Continued)

Pressure Mode

Pressure Mode Start-up at 1 mL/h (initial)

-0.2

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

1.6

1.8

2.0

0 20 40 60 80 100 120

Time (min)

(mL/h)

Pressure Mode Trumpet Curve at 1 mL/h (initial)

0.8 1.1

4.9 4.9

-6.2

2.0

-12.1

3.9

21.2 12.2

3.2

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

NOTE: The plot range has

been increased to ±100%, to

allow visualization of the graph.

Pressure Mode Trumpet Curve at 0.1 mL/h (48 hr)

-21.8

-11.9

23.8

12.3

-42.9

-7.5

-124.5

6.0

98.0

51.0

0.0

-100

-80

-60

-40

-20

100

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Legend:

n Maximum rate error

Overall rate error

u Minimum rate error

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

139

General Information

Trumpet and Start-Up Curves (Continued)

Pressure Mode (Continued)

Pressure Mode Start-up at 25 mL/h (initial)

-5

0 20 40 60 80 100 120

Time (min)

(mL/h)

Pressure Mode Start-up at 999.9 mL/h (initial)

-200

200

400

600

800

1000

1200

1400

1600

1800

2000

0 20 40 60 80 100 120

Time (min)

(mL/h)

Pressure Mode Trumpet Curve at 25 mL/h (initial)

2.3 2.2

1.8 2.1

1.3

2.0 2.1

2.2

2.9 2.5

2.2

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Pressure Mode Trumpet Curve at 999.9 mL/h (initial)

-1.4 -1.3

-0.9 -1.0 -1.1 -1.1 -1.2

-1.8 -1.3

-1.5

-1.2

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Pressure Mode Trumpet Curve at 25 mL/h (48 hr)

0.0 -0.1

-0.7 -0.3

-1.1

-0.5 -0.3

-0.10.5 0.1

-0.2

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Pressure Mode Trumpet Curve at 999.9 mL/h (24 hr)

-3.7 -3.6

-3.3 -3.4 -3.5 -3.5 -3.6

-4.0 -3.6

-3.8

-3.7

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Legend:

n Maximum rate error

Overall rate error

u Minimum rate error

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

140 General Information

Trumpet and Start-Up Curves (Continued)

Resistance Mode

Resistance Mode Start-up at 0.1 mL/h (initial)

-0.02

0.00

0.02

0.04

0.06

0.08

0.10

0.12

0.14

0.16

0.18

0.20

0 20 40 60 80 100 120

Time (min)

(mL/h)

Resistance Mode Start-up at 1 mL/h (initial)

-0.2

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

1.6

1.8

2.0

0 20 40 60 80 100 120

Time (min)

(mL/h)

Resistance Mode Trumpet Curve at 0.1 mL/h (initial)

-22.7 -19.0

43.0

18.8

-49.2

-6.3

-104.7

14.6

153.4 73.0

1.8

-100

-80

-60

-40

-20

100

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Resistance Mode Trumpet Curve at 1 mL/h (initial)

-1.4 -1.6

4.8 3.7

-11.5

-0.6

-23.4

2.6

32.6 13.3

1.2

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Resistance Mode Trumpet Curve at 0.1 mL/h (48 hr)

-22.9 -22.0

46.4

17.2

-48.9

-6.7

-109.5

13.3

173.6 74.6

-1.5

-100

-80

-60

-40

-20

100

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Resistance Mode Trumpet Curve at 1 mL/h (48 hr)

-0.6 -1.0

5.9

4.2

-11.7

0.1

-23.5

3.2

33.1 14.2

1.7

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

NOTE: The plot range has been

increased to ±100%, to allow

visualization of the graph.

Legend:

n Maximum rate error

Overall rate error

u Minimum rate error

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

141

General Information

Trumpet and Start-Up Curves (Continued)

Resistance Mode Start-up at 25 mL/h (initial)

-5

0 20 40 60 80 100 120

Time (min)

(mL/h)

Resistance Mode Start-up at 999.9 mL/h (initial)

-200

200

400

600

800

1000

1200

1400

1600

1800

2000

0 20 40 60 80 100 120

Time (min)

(mL/h)

Resistance Mode Trumpet Curve at 25 mL/h (initial)

5.0

3.2

-2.0

1.5

-8.4

-0.2

1.3

3.0

15.6

6.1

2.3

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Resistance Mode Trumpet Curve at 999.9 mL/h (initial)

-1.2 -1.1

0.1 -0.3 -0.6 -0.7 -0.7

-1.9 -1.0

-1.5

-0.9

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Resistance Mode Trumpet Curve at 25 mL/h (48 hr)

3.1

1.4

-3.6

-0.2

-9.9

-2.0

-0.5

1.2

13.4

4.1

0.5

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Resistance Mode Trumpet Curve at 999.9 mL/h (24 hr)

-3.5 -3.4

-2.7 -2.9 -3.1 -3.1

-3.9 -3.3

-3.7

-3.2

-3.3

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Resistance Mode (Continued)

Legend:

n Maximum rate error

Overall rate error

u Minimum rate error

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

142 General Information

Trumpet and Start-Up Curves (Continued)

High Resistance Mode

High Resistance Mode Start-up at 999.9 mL/h (initial)

-200

200

400

600

800

1000

1200

1400

1600

1800

2000

0 20 40 60 80 100 120

Time (min)

(mL/h)

High Resistance Mode Trumpet Curve at 999.9 mL/h (initial)

-1.4 -1.1

-0.1 0.8 0.0 -0.3

-1.3 -0.9

-2.3

-0.5

-0.7

-15

-10

-5

05 1015202530

Observation Interval (min)

Flow Rate Error (%)

High Resistance Mode Trumpet Curve at 999.9 mL/h (24 hr)

-3.9 -3.5

-2.7

-1.7

-2.5 -2.8

-4.7 -3.3

-3.7

-3.0

-3.1

-15

-10

-5

0 5 10 15 20 25 30

Observation Interval (min)

Flow Rate Error (%)

Legend:

n Maximum rate error

Overall rate error

u Minimum rate error

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

143

Troubleshooting and Maintenance

General

The SE Pump Technical Service Manual is available from

Cardinal Health. It includes routine service schedules,

interconnect diagrams, component parts lists and descriptions,

test procedures, and other technical information, to assist

qualified service personnel in repair and maintenance of the

instrument’s repairable components. Maintenance procedures

are intended to be performed only by qualified personnel.

Artifacts: It is normal for an infusion device to produce

nonhazardous currents when infusing electrolytes. These

currents vary proportional to the infusion device flow rate.

When an ECG monitoring system is not functioning under

optimal conditions, these currents may appear as artifacts,

simulating actual ECG readings. To determine if ECG

abnormalities are caused by patient condition or the ECG

equipment, place the infusion device on hold. If the ECG

readings become normal, the ECG equipment requires

attention. Proper setup of the ECG equipment should

eliminate these artifacts. Reference the appropriate ECG

monitoring system documentation for instructions on setup and

maintenance.

Air In Line Assembly

The Air-in-Line Detection System provides clinicians the

ability to detect inappropriate amounts of air in the IV line.

The instrument is configurable to allow single bubble and

accumulated air detection. Accumulated air detection is based

on measurement of the average percentage produced by small

air bubbles passing the detector. À

Air is detected by an emitter (Air-in-Line arm) which rotates

into position as the latch is closed. A receiver (Air-in-Line

Detector), opposite the arm and just below the Pumping

Mechanism, sends the Air-in-Line information to the main

processor.

Qualified biomedical personnel may configure 1 of 4 possible

sensitivity levels. The instrument is also configurable to

permit the operator to clear (reset) any air registered in the

instrument’s memory.

Air-in Line Arm

Air-in Line Detector

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

144 Troubleshooting and Maintenance

Air In Line Assembly (Continued)

1. To place channel on hold, press hold soft key.

2. Remove air per hospital protocol. À

3. To resume infusion, reinstall set and then press RUN/

HOLD key.

If air volume is clinically insignificant, press reset soft key

or RUN/ HOLD key, followed by run soft key or RUN/

HOLD key to resume infusion.

• Subsequent air bubbles trigger alarm.

NOTE:

À Ensure that the tubing is properly inserted into the air detector

to avoid false alarms. The tubing may be reshaped to ensure

optimum contact with the sensors. Periodically clean the Air-

in-Line Detector to ensure a clear signal can be received (see

“Cleaning”).

Single or Accumulated Air Bubble Detection (NO Reset Feature)

NOTE:

À Opening the latch or turning the channel off clears air

memory.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

145

Troubleshooting and Maintenance

Alarms, Alerts, Prompts

There are 3 types of displayed messages listed on the

following pages with a probable cause and suggested remedy

next to each one. Use this section in conjunction with the

appropriate clinical practice of hospital procedure. Additional

information can be found in other sections of this DFU (see

"Table of Contents"). Use this section in conjunction with the

appropriate clinical practice or hospital procedure.À

ALARM: instrument or channel problem.

• infusion stops

• alarm bell icon illuminates

• alarm tone sounds

• rate LED display flashes

• message appears in Main Display when channel is

selected

ALERT: may indicate a change in infusion status.

• channel continues to operate

• alert tone sounds

• message appears in Main Display

PROMPT: infusion status not changed.

Startup procedures were not completed or an invalid key was

pressed.

NOTE:

À When using the dual channel instrument, some messages

also display Channel A or Channel B, to indicate which

channel is affected. Always verify the channel is selected

before making any changes.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

146 Troubleshooting and Maintenance

BATTERY DEPLETED (Plug In) Battery is too low to operate

instrument.

Plug power cord into an AC

outlet immediately. Press

run soft key or RUN/HOLD to

resume infusion.

Alarms, Alerts, Prompts (Continued)

Alarms

ACCUMULATED AIR IN LINE Air detector has detected

multiple small bubbles.

Press hold soft key. Open

latch to remove set. Clear air

per hospital protocol. Reinstall

set. Press Run/Hold to resume

infusion.

If reset key is active and

air bubbles are clinically

insignificant, press reset soft

key and then press run soft key

to resume infusion.

Ensure air-in-line sensors are

thoroughly cleaned.

AIR IN LINE Air detector has detected an air

bubble larger than configured

threshold tolerance.

Press hold soft key. Open latch

to remove set. Clear air per

hospital protocol. Reinstall set.

Press RUN/HOLD to resume

infusion.

If reset key is active and

air bubbles are clinically

insignificant, press reset soft

key and then press run soft key

to resume infusion.

At flow rates of 1.0 mL/h and

below, verify upstream fluid path

is unobstructed.

Ensure air-in-line sensors are

thoroughly cleaned.

Alarm Meaning Response

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

147

Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Alarms (Continued)

CHANNEL MALFUNCTION

Dual channel instrument

only.

Channel malfunction. Turn channel off and then on.

If problem persists, do not use

channel. Contact qualified

service personnel.

FLOW SENSOR UNPLUGGED Flow sensor is unplugged from

back of instrument.

Plug flow sensor into flow

sensor receptacle.

COMPUTER LINK FAILURE RS-232 connection to computer

was disrupted.

Computer Link feature is in

monitor mode.

Check RS-232 connections.

Clearing this alarm

automatically puts instrument

in monitor mode. Reestablish

infusion.

HOLD TIME EXCEEDED Channel has been on hold for 2

minutes and no keys have been

pressed (on either channel if

dual channel).

Press hold soft key to return to

hold mode.

INSTRUMENT MALFUNCTION Instrument malfunction. For a

dual channel instrument, neither

channel is functional.

Turn instrument off and then on.

If problem persists, do not use

instrument. Contact qualified

service personnel.

KEY STUCK A key is stuck or was held down

too long.

Release key. Turn instrument

off (both channels if dual

channel instrument) and then

on. If problem persists, do

not use instrument. Contact

qualified service personnel.

LATCH OPEN Latch was opened during an

infusion.

Check for proper set installation.

Close latch fully to the left.

Press run soft key.

Alarm Meaning Response

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

148 Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Alarms (Continued)

NO UPSTREAM FLOW

DETECTED

Flow has been obstructed

between container and

instrument when using a flow

sensor.

Check to see if container

is empty, flow sensor is

mispositioned or clouded, tubing

is kinked or air vent is closed.

Verify correct set connections

and open fluid path. Press run

soft key to restart infusion. À

OCCLUSION DOWNSTREAM Pressure in IV line has

exceeded a pressure alarm

threshold.

Resistance has reached 100%.

Check administration set for

probable cause (such as kinked

tubing, closed stopcock, high

resistance catheter). Press run

soft key to restart infusion.

OCCLUSION UPSTREAM Flow has been obstructed

between fluid container and

instrument's pressure sensor.

Check administration set for

probable cause (such as kinked

tubing, closed clamp). Verify

that blue thumb clamp on Flow

Regulator has moved to open

(up) position. If not, reload set.

Press run soft key to restart

infusion.

Alarm Meaning Response

NOTE:

À Infusing fluids which form smaller drops through a 60 drops/mL

set at high rates may result in a No Upstream Flow Detected

alarm. (This is because the small, rapidly falling drops form a

continuous stream which does not trigger the flow sensor). In

this event, unplug the flow sensor from the instrument.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

149

Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Alarms (Continued)

PRIMARY FLOW DETECTED

DURING SECONDARY

Instrument detected flow

from primary container

during secondary infusion.

NOTE: Alarm can only occur

when using optional flow

sensor.

Verify that flow sensor is on

Primary line and that set up is

correct.

SETUP TIME EXCEEDED Instrument has been turned on

but no keys have been pressed

for 10 minutes.

Press hold soft key to return to

hold mode.

Instrument turns off if left in

alarm more than 5 minutes.

If an audio alarm remains on,

turn instrument on and then off.

SET OUT Set has been removed during

an infusion.

Reinstall set. Press run soft

key to restart infusion

Alarm Meaning Response

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

150 Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Alerts

Battery Low Battery has 30 minutes or less

of charge remaining.

Plug power cord into an AC

outlet as soon as possible.

Checking Line Flow has been obstructed.

Auto Restart Plus feature is on.

Auto Restart Plus feature must

be on for downstream occlusion

alerts (not required for upstream

occlusion alerts). Check

administration set for probable

cause (such as kinked tubing,

clogged filter, etc.).

Complete Entry ENTER was not pressed to

accept a new value.

Press ENTER to confirm entry

or press CLEAR twice to return

to previous settings.NOTE:

Channel operates as previously

programmed until ENTER is

pressed.

Resistance Alert IV line resistance has reached

preset alert level.

Resistance Alert feature is on.

Check downstream line and

site. Raise resistance alert

level, if appropriate.

Additional Alerts:

Additional alerts provide notification of program completion and/or transition to another mode: Bolus Dose

Complete, Dose Complete (Multi-Dose Mode), Loading Dose Complete, Multi-Step Complete, Secondary

Complete, Infusion in KVO or VTBI = 0.)

Alert Meaning Response

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

151

Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Prompts

Entry Invalid An invalid value was entered

during programming.

Press CLEAR or 0 key to clear

entry. Enter appropriate value.

Dose Out of Range Calculated dose is outside

allowable range.

Verify and reenter settings.

Invalid Entry Rate Out of

Range

Instrument has calculated a rate

less than 0.1 mL/h.

Verify and reenter settings.

Instrument Self-Check Is Due

Please Eject the Set

Instrument/channel has not

performed self-check within

programmed interval.

If set is loaded: Eject set, wait 5

seconds and then reload set.

If no set is loaded: Load set,

wait 1 minute and then eject

set. Wait 5 seconds and then

reload set.

Maintenance Reminder Periodic maintenance interval

has elapsed.

Maintenance Reminder feature

is on.

Notify Biomedical Engineering

department. If desired, press

continue soft key to temporarily

bypass reminder.

Latch Open Latch is open (prior to starting

an infusion).

Close latch fully to left.

Air In Line Air detector has detected air

prior to starting infusion or is in

poor contact with set.

Press continue soft key to

allow infusion to continue. An

alarm occurs if air detector

detects an air bubble larger

than configured threshold.

Verify set is loaded correctly.

Prime and reload set or remove

air. Reshape tubing to ensure

optimum contact with sensor.

Ensure air-in-line sensors are

thoroughly cleaned.

Prompt Meaning Response

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

152 Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Prompts (Continued)

New Baseline Set A new Manual Pressure

Baseline was successfully set.

Manual Pressure Baseline

feature is on.

Baseline remains set until a

new manual baseline is set,

instrument is turned off or latch

is opened.

Occlusion Downstream A very high pressure exists in

fluid line while baseline is being

set.

Pressure Baseline feature is on.

Remove source of high

pressure and repeat setting of

pressure baseline.

Panel Locked A key was pressed.

Panel lock feature is on.

Turn panel lock off to access

panel controls. Panel lock key

is located behind handle.

Ok Entry Attempt was made to go to

another page before pressing

ok soft key.

Verify all parameters are correct

and press ok soft key.

Place on Hold to Set Pressure

Baseline

SET PRESSURE BASELINE

function was selected while

running.

Pressure Baseline feature is on.

Place instrument on hold

before performing manual

SET PRESSURE BASELINE

operation.

Press and Hold Key to Turn

Off

POWER was pressed. Press and hold POWER until

display turns off.

Max Rate = XXX.X mL/h

(XXX.X represents maximum

flow rate configured for

instrument or profile.)

An attempt was made to enter

a rate greater than maximum

configured rate or instrument

has calculated a rate greater

than maximum configured

rate. Default maximum rate is

999.9 mL/h in primary mode,

600 mL/h in secondary mode.

Verify and reenter settings.

Prompt Meaning Response

Place on Hold to Change A key was pressed during KVO. Channel must be on hold to

make changes.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

153

Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Prompts (Continued)

Pressure Limit XXX mmHg

(XXX represents configured

maximum pressure)

An elevated pressure was

present in fluid path when

pressure baseline was

established. This may reduce

maximum available pressure

range.

Reload administration set and

verify no obstruction exists

which could cause excess

pressure.

• If Pressure Baseline feature

is on, repeat manual setting

of pressure baseline.

OTHERWISE

• Restarting infusion

automatically sets pressure

baseline.

Pressure Limit Must Be Less

Than or Equal to XXX mmHg

(XXX represents configured

maximum pressure)

Attempt was made to increase

pressure alarm limit to a

level higher than configured

maximum pressure.

Choose a pressure alarm limit

that is less than, or equal to,

configured maximum pressure.

Pressure Unstable Cannot

Set Baseline

Excessive variation in pressure

due to motion, flow from other

instruments or blood pressure

prevents accurate setting of

pressure baseline.

Pressure Baseline feature is on.

Reduce or temporarily remove

sources of variation while

performing manual baseline

setting operation.

Program Lost Re-Enter

Settings

Instrument detected a memory

or power failure. Existing

operating parameters were

erased.

Press continue soft key and

reenter all infusion settings.

Configurable options are not

affected.

Rate Out of Range Instrument has calculated a rate

less than 0.1 mL/h.

Verify and reenter settings.

Set Must Be Loaded Flow Regulator segment is not

loaded in selected channel

during a manual pressure

baseline setting operation.

Pressure Baseline feature is on.

Load Flow Regulator segment

in selected channel. Repeat

manual pressure baseline

setting.

Prompt Meaning Response

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

154 Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Prompts (Continued)

Set Out Flow Regulator segment is not

installed correctly.

Reinstall Flow Regulator

segment.

Set Pri VTBI > Loading Dose

VTBI

Loading Dose VTBI entered is

greater than primary VTBI.

Raise primary VTBI or lower

Loading Dose VTBI, as

appropriate.

Set Pressure Baseline Set Pressure Baseline was

selected in options mode.

Press ok soft key to set

Pressure Baseline or press

return soft key to go to exit.

Set Pri VTBI A primary VTBI was not

programmed.

Enter a primary VTBI.

Stop Timer to Change An invalid key was pressed

while timer was running in Multi-

Dose program.

Wait several seconds for popup

to finish. Press stop timer soft

key to make changes.

Stop Secondary and Infuse

Primary?

Run soft key was pressed

in Primary Mode when a

secondary infusion was on hold.

If return to primary parameters

is appropriate press yes soft

key. If continued secondary

infusion is appropriate, press no

soft key.

The Specified VTBI Will Only

Deliver a Partial Dose

Secondary VTBI value is

significantly less than bag

volume programmed on set up

page.

Verify parameters are correct.

Press yes soft key to proceed

or no soft key to return to

programming.

Time Out of Range Programmed step time exceeds

24 hours and 59 minutes, or is

less than 1 minute.

Verify and reenter settings.

Prompt Meaning Response

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

155

Troubleshooting and Maintenance

Alarms, Alerts, Prompts (Continued)

Prompts (Continued)

Invalid Keypress During Programming:

The following Prompts may be seen if an invalid key is pressed during programming: Both A and B not

Running, Channel Not On, Complete or OK Setup, No Numeric Entries, Select Channel.

Invalid Keypress During Infusion:

During an infusion, if an invalid key is pressed, the following prompts may be seen: Dose Rate Running,

Loading Dose Running, Multi-Dose Running, Multi-Step Running, Pri Running, Sec Running, or Timer

Running (Multi-Dose program).

Resuming Previous Programming:

When an instrument has been powered off then on again previous parameters may be preserved if

Current Profile is accepted and New Patient? – No is selected. The following prompts may be seen:

Return to Dose Rate?, Return to Loading Dose?, Return to Multi-Dose?, Return to Multi-Step?, or

Return to Secondary?.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

156 Troubleshooting and Maintenance

Inspection Requirements

To ensure the system remains in good operating condition,

both regular and preventive maintenance inspections are

required.

WARNING

Failure to perform these

inspections may result in improper

instrument operation.

CAUTIONS

• Regular and preventive

maintenance inspections should

only be performed by qualified

service personnel.

• Inspect LCD for anomalies

(improperly lit/unlit pixels).

REGULAR INSPECTIONS

PROCEDURE FREQUENCY

INSPECT FOR DAMAGE:

Case

Connector

Keypad

Each usage

CLEANING As required

START UP Each usage

Cleaning

DO NOT use solutions containing phosphoric acid (Foamy

Q&A À), aromatic solvents (naphtha, paint thinner,

etc.), chlorinated solvents À (Trichloroethane, MEK,

Toluene, etc.), ammonia, acetone, benzene, xylene

or alcohol, other than as specified below.

DO NOT use hard or pointed objects to clean any part of

instrument.

DO NOT use pressurized sprays on instrument.

Acceptable cleaning solutions are (use per manufacturers’

instructions):

10% bleach solution (1 part bleach to 9 parts water)

Vesphene

Manu-Klenz

Warm water

1. Unplug power cord from AC outlet before cleaning.

2. Verify RS-232 connector is covered. Do not spray fluid

directly into any connector.

Turn the instrument off and unplug

the power cord from AC power

before cleaning. Do not spray

fluids directly onto the instrument.

Do not steam autoclave, EtO

sterilize, immerse the instrument or

allow fluids to enter the instrument

case. Failure to follow these

instructions may result in an

electrical hazard.

WARNING

The solutions/solvents identified

as NOT to be used can damage the

surfaces of the instrument.

CAUTION

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

157

Troubleshooting and Maintenance

Cleaning (Continued)

3. Use a soft cloth dampened with warm water and a mild,

nonabrasive cleaning solution.

• A soft-bristled brush may be used to clean narrow

areas.

• Use light pressure when cleaning pressure transducer

and air-in-line detector areas of pumping channels.

4. Flow sensor should be routinely cleaned by running warm

water over it while actuating slider, and then thoroughly

dried.

NOTE:

À Excluding 10% bleach solution in water.

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

158 Troubleshooting and Maintenance

If the instrument shows evidence of damage in transit, notify

the carrier’s agent immediately. Do not return damaged

equipment to the factory before the carrier’s agent has

authorized repairs.

If the instrument fails to respond as described in this

document and the cause cannot be determined, do not use

the instrument. Contact qualified Cardinal Health service

personnel.

If it is necessary to return the instrument for service, obtain

a return authorization number prior to shipment. Carefully

package the instrument (preferably in the original packaging),

reference the return authorization information, and return it to

the appropriate service or distribution center. Cardinal Health

does not assume any responsibility for loss of, or damage to,

returned instruments while in transit.

Service Information

• The instrument case should only

be opened by qualified personnel

using proper grounding

techniques. Prior to performing

maintenance, disconnect SE

Pump from AC power.

• During servicing, an instrument’s

configuration settings might

be reset to the factory defaults.

Qualified hospital/facility

personnel are responsible for

checking in the instrument and

ensuring the current hospital-

approved Data Set is loaded

if Guardrails® Suite MX is in

use, or that instrument system

configuration settings are correct

if the Profiles feature is set to

OFF.

WARNINGS

Technical support, service information, applications, and

manuals may be obtained by contacting a Cardinal Health

representative.

When submitting any request for service, include:

• model number

• a description of difficulty experienced

• instrument settings

• administration set/lot number

• solution(s) used

• message displayed at time of difficulty

Technical Support

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

159

Troubleshooting and Maintenance

Cardinal Health warrants that:

A. Each new SE Pump is free from defects in material and workmanship under normal use and

service for a period of one (1) year from the date of delivery by Cardinal Health to the original

purchaser.

B. The battery and each new accessory is free from defects in material and workmanship under

normal use and service for a period of ninety (90) days from the date of delivery by Cardinal

Health to the original purchaser.

If any product requires service during the applicable warranty period, the purchaser should

communicate directly with Cardinal Health to determine the appropriate repair facility. Except as

provided otherwise in this warranty, repair or replacement will be carried out at Cardinal Health’s

expense. The product requiring service should be returned promptly, properly packaged and

postage prepaid by purchaser. Loss or damage in return shipment to the repair facility shall be at

purchaser’s risk.

In no event shall Cardinal Health be liable for any incidental, indirect or consequential damages

in connection with the purchase or use of any SE Pump product. This warranty shall apply

solely to the original purchaser. This warranty shall not apply to any subsequent owner or holder

of the product. Furthermore, this warranty shall not apply to, and Cardinal Health shall not be

responsible for, any loss or damage arising in connection with the purchase or use of any SE

Pump product which has been:

1. repaired by anyone other than an authorized Cardinal Health Service Representative;

2. altered in any way so as to affect, in Cardinal Health’s judgment, the product’s stability or

reliability;

3. subjected to misuse or negligence or accident, or which has had the product’s serial or lot

number altered, effaced or removed; or

4. improperly maintained or used in any manner other than in accordance with the written

instructions furnished by Cardinal Health.

This warranty is in lieu of all other warranties, express or implied, and of all other obligations or

liabilities of Cardinal Health, and Cardinal Health does not give or grant, directly or indirectly, the

authority to any representative or other person to assume on behalf of Cardinal Health any other

liability in connection with the sale or use of SE Pump products.

CARDINAL HEALTH DISCLAIMS ALL OTHER WARRANTIES, EXPRESS OR IMPLIED, INCLUDING

ANY WARRANTY OF MERCHANTABILITY OR OF FITNESS FOR A PARTICULAR PURPOSE OR

APPLICATION.

See packing inserts for international warranty, if applicable.

WARRANTY

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

160 Troubleshooting and Maintenance

THIS PAGE

INTENTIONALLY

LEFT BLANK

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

161

Regulations and Standards

Compliance

This system complies with part 18 of the FCC Rules. Operation

is subject to the following 2 conditions:

• This system may not cause harmful interference.

• This system must accept any interference received,

including interference that may cause undesired operation.

The digital apparatus does not exceed the Class B limits for

radio noise emissions from digital apparatus set out in the

radio interference regulations of the Canadian Department of

Communications (DOC).

Le present appareil numerique n'emet pas de bruits

radiolelectriques depassant les limites applicables aux

appareils numeriques de la Classe A/B prescrites dans le

reglement sur le brouillage radioelectrique edicte par le

Ministere des Communications du Canada.

This system has been tested and found to comply with either

the limits for a Class B digital device (without Model 180 Flow

Sensor), or as a Class A digital device (with Model 180 Flow

Sensor), pursuant to Part 18 of the FCC Rules. These limits

are designed to provide reasonable protection against harmful

interference when the system is operated in a commercial

environment. This system generates, uses, and can radiate

radio frequency energy. If it is not installed and used in

accordance with the applicable directions for use, it may cause

harmful interference to radio communications. Operation

of this system in a residential area is likely to cause harmful

interference, in which case the user will be required to correct

the interference at their own expense.

The authority to operate this system is conditioned by the

requirement that no modifications will be made to the system

unless the changes or modifications are expressly approved by

Cardinal Health, Inc.

This Class A/B digital apparatus meets all requirements of the

Canadian Interference-Causing Equipment Regulation.

Cet appareil numerique de la Classe A/B respecte toutes les

exigences du Reglement sur le materiel brouilleur du Canada.

Electromagnetic Environment

Any changes or modifications not

expressly approved by the personnel

responsible for compliance could

void the user's authority to operate

the system.

CAUTION

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

162 Regulations and Standards

Compliance (Continued)

Electromagnetic Environment (Continued)

Tables: The SE Pump is intended for use in the

electromagnetic environments specified in the following tables.

Table 1

Electromagnetic Emissions

Emissions Test Compliance Electromagnetic Environment - Guidance

CISPR 11

RF Emissions

Group 1

Class B

The SE Pump is suitable for use in all establishments, including

domestic establishments and those directly connected to a public

low-voltage power supply network that supplies buildings used for

domestic purposes.

IEC 61000-3-2

Harmonic Emissions Class A

IEC 61000-3-2

Voltage Fluctuations

Flicker Emissions

Complies

Group 1

Class A

The SE Pump is intended for use under the supervision of healthcare

professionals only. This is a CISPR 11 Class A when the Model 180

(Flow Sensor) accessory is used and a CISPR 11 Class B when

the Model 180 is not used. In a domestic environment, this system

may cause radio interference. Reorienting, relocating or shielding

the system, or filtering the connection to the public mains network,

are examples of steps that can be taken to reduce or eliminate

interference.

The SE Pump is suitable for use in all establishments, including

domestic establishments and those directly connected to a public

low-voltage power supply network that supplies buildings used for

domestic purposes, provided the following Caution is heeded:.

CISPR 11

RF Emissions

CAUTION

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

163

Regulations and Standards

Compliance (Continued)

Table 2

Electromagnetic Immunity

IEC 61000-4-2

Electrostatic

Discharge (ESD)

Floors should be wood, concrete, or ceramic tile.

If floors are covered with synthetic material,

relative humidity should be at least 30%.

If connector testing exemption is used, following

ESD sensitivity symbol appears adjacent to each

connector. " - Do Not Touch"

Emissions Test Electromagnetic Environment - Guidance

±6 kV contact

±8 kV air

IEC 60601-1-2

Test Level

±8 kV contact À

±15 kV air À

Compliance

Level

IEC 61000-4-4

Electrical Fast

Transient, Burst

(EFT) Á

Mains power quality should be that of a typical

commercial or hospital environment.

±2 kV for power

supply lines

±1 kV for input/

output lines

±2 kV for power

supply lines

±1 kV for input/

output lines

IEC 61000-4-5

Power Line Surge Á

Mains power quality should be that of a typical

commercial or hospital environment.

±1 kV differential

mode

±2 kV common

mode

±1 kV differential

mode

±2 kV common

mode

IEC 61000-4-8

Power Frequency

Magnetic Field

(50/60 Hz)

Power frequency magnetic fields should be at

levels characteristic of a typical location in a

typical commercial or hospital environment.

3 A/m 400 A/m 50 Hz À

400 A/m 60 Hz À

Electromagnetic Environment (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

164 Regulations and Standards

IEC 61000-4-11

Voltage Dips, Short

Interruptions, and

Voltage Variations Á

Mains power quality should be that of a typical

commercial or hospital environment.

If continued operation of the SE Pump is

required during power mains interruptions, it is

recommended that the SE Pump be powered

from an uninterruptible power supply or a battery.

The SE Pump does employ an internal short

duration battery.

<5% UT

(>95% dip in UT)

for 0.5 cycle

40% UT

(60% dip in UT)

for 5 cycles

70% UT

(30% dip in UT)

for 25 cycles

<5% UT

(>95% dip in UT)

for 5 sec

<5% UT

(>95% dip in UT)

for 0.5 cycle

40% UT

(60% dip in UT)

for 5 cycles

70% UT

(30% dip in UT)

for 25 cycles

<5% UT

(>95% dip in UT)

for 5 sec

Table 2 (Continued)

Electromagnetic Immunity

Emissions Test Electromagnetic Environment - Guidance

IEC 60601-1-2

Test Level Â

Compliance

Level Â

Compliance (Continued)

Electromagnetic Environment (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

165

Regulations and Standards

IEC 61000-4-6

Conducted RF

IEC 61000-4-3

Radiated RF

Portable and mobile RF communications equipment

should be used no closer to the SE Pump (including

cables) than recommended separation distance

calculated from equation applicable to frequency of

transmitter.

Recommended Separation Distance

— d = [-----] √P

— d = [-----] √P 80 MHz - 800 MHz

— d = [-----] √P 80 MHz - 2.5 GHz

d = recommended separation distance in

meters (m). Å

P = maximum output power rating of transmitter in

watts (W) according to transmitter manufacturer.

Field strengths from fixed RF transmitters, as

determined by an electromagnetic site survey,

should be less than compliance level in each

frequency range. Æ Ç

Interference may occur in vicinity of equipment

marked with following symbol:

3 Vrms

150 kHz - 80 MHz

3 V/m

80 MHz - 2.5 GHz

10 Vrms

10 V/m

Table 3

Electromagnetic Immunity - Life Support Equipment

Immunity Test Electromagnetic Environment - Guidance Ã Ä

IEC 60601-1-2

Test Level

Compliance

Level À

Compliance (Continued)

Electromagnetic Environment (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

166 Regulations and Standards

Rated Maximum

Output Power of

Transmitter (W)

150 kHz - 80 MHz

Outside ISM

Bands

3.5

— d = [-----] √P

150 kHz - 80 MHz

In ISM Bands

— d = [-----] √P

80 MHz - 800 MHz

— d = [-----] √P

800 MHz - 2.5 GHz

— d = [-----] √P

0.01

0.1

100

0.04

0.11

0.35

1.11

3.5

0.12

0.38

1.2

3.8

0.12

0.38

1.2

3.8

0.23

0.73

2.3

7.3

Separation Distance Based on Transmitter Frequency (m)

Table 4 Ã Ä Å È

Recommended Separation Distances

Reduce the potential for electromagnetic interference by maintaining a minimum distance between

portable and mobile RF communications equipment (transmitters) and the SE Pump as recommended

in this table, based on the maximum output power of the communications equipment.

For transmitters rated at a maximum output power not listed in this table, the recommended separation

distance (d) in meters (m) can be determined using the equation applicable to the frequency of the

transmitter, where P is the maximum output power rating of the transmitter in watts (W) based on the

transmitter manufacturer.

Compliance (Continued)

Electromagnetic Environment (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

167

Regulations and Standards

NOTES:

À Compliance levels raised by IEC 60601-2-24.

Á Performed at the minimum and maximum rated input voltage.

Â UT is the AC mains voltage prior to application of the test level.

Ã At 80 MHz and 800 MHz, the higher frequency range applies.

Ä These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption

and reflection from structures, objects and people.

Å The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz, and in the frequency

range 80 MHz - 2.5 GHz, are intended to decrease the likelihood that mobile/portable communications

equipment could cause interference if inadvertently brought into patient areas. For this reason, an

additional factor of 10/3 is used in calculating the recommended separation distance for transmitters in

these frequency ranges.

Æ Field strengths from fixed transmitters [such as base stations for radio (cellular/cordless) telephones and

mobile radios, amateur radio, AM/FM radio broadcast, TV broadcast] cannot be predicted theoretically with

accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site

survey should be considered. If the measured field strength in the location in which the SE Pump is used

exceeds the applicable RF compliance level, the SE Pump should be observed to verify normal operation.

If abnormal performance is observed, additional measures may be necessary, such as reorienting or

relocating the SE Pump.

Ç Over the frequency range 150 kHz - 80 MHz, field strengths should be less than [V1] V/m.

È The ISM (Industrial, Scientific and Medical) bands between 150 kHz and 80 MHz are 6.765 - 6.795 MHz,

13.553 - 13.567 MHz, 26.957 - 27.283 MHz, and 40.66 - 40.70 MHz.

Compliance (Continued)

Electromagnetic Environment (Continued)

Directions for Use

Alaris® SE Pump

Models 7130/7131, 7230/7231

168 Regulations and Standards

Compliance (Continued)

The SE Pump has been assessed and complies with the

following standards:

IEC EN 60601–1 / BS 5724, including amendments A1 and

A2; IEC EN 60601–2–24; CISPR 11, Group 1, Class A/B

Emissions; IEC EN 60601–1–2, UL 60601-1, CAN/CSA No.

601.1-M90

Standards

Trademarks

Alaris®, AccuSlide®, Guardrails® and SmartSite® are registered

trademarks of Cardinal Health, Inc. or one of its subsidiaries.

All other trademarks belong to their respective owners.

Supplemental Information:

Signature Edition®GOLD Infusion System,

Model 180 Empty Container Detector (ECD)

This document provides supplemental information on emissions testing specifications located in

Specifications section of Maintenance chapter of the Signature Edition® GOLD Infusion System

Directions For Use.

NOTES: The Signature Edition® GOLD infusion system has been assessed and complies with the

following Technical Standards: IEC EN 60601-1 including amendments A1 and A2; IEC EN 60601-

1-2: 2002; IEC EN 60601-2-24; CISPR 11, Group 1. Class A requirements are met with use of

ECD/flow sensor. Class B emissions requirements are met without use of ECD/flow sensor.

Class A Emission Statement:

Instrument used with an ECD/flow sensor, is suitable for use in all establishments other than

domestic and those directly connected to public low-voltage power supply network supplying

buildings used for domestic purposes. However, the Instrument may be used in domestic

establishments with additional necessary (appropriate) measures.

Class B Emission Statement:

Instrument used without an ECD/flow sensor, is suitable for use in all establishments, including

domestic establishments and those directly connected to public low-voltage power supply network

supplying buildings used for domestic purposes.

This Signature Edition® GOLD Infusion System is intended for use by Healthcare Professionals

only. This is a CISPR 11, Class A Medical equipment/system when Model 180 accessory is used.

In a domestic environment this equipment/system may cause radio interference, and may be

necessary to take adequate mitigation measures, such as rearrange, relocate or shield the

Signature Edition® System or filter the connection to public mains network.

ALARIS®, ALARIS Medical Systems®, Signature Edition® are registered trademarks of ALARIS Medical

Systems, Inc. All other trademarks belong to their respective owners.

P/N 10010613

CAUTION

Models 7130/7131 and 7230/7231

(With Guardrails®Safety Software or

Guardrails®Safety Software Compatible)

OPTIONS

SEC

PRI

POWER

RUN

HOLD

Clear Enter

PRI SEC HLD OPT KVO

HLD PRI SECKVO OPT

456

789

•0

POWER

RUN

HOLD

A B

ml/hr ml/hr

Directions for Use

SUPPLEMENT

Signature Edition®GOLD Infusion System

Cardinal Health,

1180 Rolle,

Switzerland

www.cardinal.com/uk/alaris

Alaris® Products

SEC

PRI

Clear Enter

OPT PRI HLD SEC KVO

RUN

HOLD

POWER

OPTIONS

456

789

ml/hr

OPTIONS

SEC

PRI

POWER

RUN

HOLD

Clear Enter

PRI SEC HLD OPT KVO

HLD PRI SECKVO OPT

456

789

•0

POWER

RUN

HOLD

A B

ml/hr ml/hr

Directions for Use

Supplement

Alaris® SE Pump

Models 71XX, 72XX

December 2006

General Contact Information

Directions for Use Supplement

Alaris® SE Pump

Models 71XX, 72XX

For service contact your local Affiliate Office or Distributor.

Cardinal Health,

PO Box 5527,

Dubai, United Arab Emirates.

Tel: (971) 4 28 22 842

Fax: (971) 4 28 22 914

Cardinal Health,

Pascalstr. 2,

52499 Baesweiler,

Deutschland.

Tel: (49) 2401 604 0

Fax: (49) 2401 604 121

Cardinal Health,

Via Ticino 4,

50019 Sesto Fiorentino,

Firenze, Italia.

Tél: (39) 055 30 33 93 00

Fax: (39) 055 34 00 24

Cardinal Health

10221 Wateridge Circle,

San Diego, CA 92121,

USA.

Tel: (1) 800 854 7128

Fax: (1) 858 458 6179

Cardinal Health,

8/167 Prospect Highway,

Seven Hills, NSW 2147,

Australia.

Tel: (61) 2 9838 0255

Fax: (61) 2 9674 4444

Fax: (61) 2 9624 9030

Cardinal Health,

Avenida Valdeparra 27,

28108 - Alcobendas, Madrid,

España.

Tel: (34) 91 657 20 31

Fax: (34) 91 657 20 42

Cardinal Health,

Kantorenpand “Hoefse Wing”,

Printerweg, 11,

3821 AP Amersfoort,

Nederland.

Tel: (31) 33 455 51 00

Fax: (31) 33 455 51 01

Cardinal Health,

Unit 2 Oude Molen Business

Park,

Oude Molen Road, Ndabeni,

Cape Town 7405, South Africa.

Tel: (27) (0) 860 597 572

Tel: (27) 21 510 7562

Fax: (27) 21 5107567

Cardinal Health,

Otto De Mentockplein 19,

1853 Strombeek - Bever,

Belgium.

Tel: (32) 2 267 38 99

Fax: (32) 2 267 99 21

Cardinal Health,

Immeuble Antares - Technoparc,

2, rue Charles-Edouard Jeanneret.

78300 POISSY,

France.

Tél: (33) 1 30 06 74 60

Fax: (33) 1 39 11 48 34

Cardinal Health

Solbråveien 10 A,

1383 ASKER,

Norge.

Tel: (47) 66 98 76 00

Fax: (47) 66 98 76 01

Cardinal Health,

235 Shields Court,

Markham,

Ontario L3R 8V2,

Canada.

Tel: (1) 905-752-3333

Fax: (1) 905-752-3343

Cardinal Health,

The Crescent, Jays Close,

Basingstoke,

Hampshire, RG22 4BS,

United Kingdom.

Tel: (44) 0800 917 8776

Fax: (44) 1256 330860

Cardinal Health,

14 George Bourke Drive

Mt Wellington, Auckland

PO Box 14234

Panmure, Auckland

Tel: 09 270 2420

Freephone: 0508 422734

Fax: 09 270 6285

Cardinal Health,

Shanghai Representative Office,

Suite 9B,

Century Ba-Shi Building,

398 Huai Hai Rd(M.),

Shanghai 200020,

China.

Tel: (56) 8621-63844603

Tel: (56) 8621-63844493

Fax: (56) 8621-6384-4025

Cardinal Health,

Döbrentei tér 1,

H-1013 Budapest,

Magyarország.

Tel: (36) 14 88 0232

Tel: (36) 14 88 0233

Fax: (36) 12 01 5987

Cardinal Health,

Hammarbacken 4B,

191 46 Sollentuna,

Sverige.

Tel: (46) 8 544 43 200

Fax: (46) 8 544 43 225

Introduction

About This Document

This supplemental Directions for Use (DFU) provides an

update to the Alerts information found in the "Troubleshooting

and Maintenance" chapter in the applicable DFU for each

Alaris® SE single and SE dual channel pump (formerly known

as the Signature Edition® Infusion System).

WARNING

Before using the Alaris® SE pump,

read all instructions in the

applicable DFU.

Alert

The following Alert is in addition to those provided in the

applicable Alaris® SE pump DFU.

Alert Meaning Response

CHECK ENTRY Key press unclear. press Clear key

to continue

• Listen to Audible Tones.

• Verify Screen Displays

Verify prescribed therapy on display screen prior to starting

or restarting an infusion.

• Observe Flow Rate

Observe the IV tubing drip chamber to verify expected flow.

Important Notes

WARNING

Verify all programming parameters

on the display screen are correct

prior to initiating RUN/HOLD.

Directions for Use Supplement

Alaris® SE Pump

Models 71XX, 72XX

2Introduction

Alaris® is a registered trademark of Cardinal Health,Inc. or one of its subsidiaries.

Trademarks

Directions for Use Supplement

Alaris® SE Pump

Models 71XX, 72XX

Direction for Use

Alaris® SE Pump

Models 7130/7131, 7320/7231

Cardinal Health,

1180 Rolle,

Switzerland

www.cardinal.com/uk/alaris

Alaris SE DFU V8.5 7131 User Manual

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